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GENE - TERM ANNOTATION REPORT

326 Annotations Found.

An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151824288 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151771455 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151781345 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126741435 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:16199547 PMID:25741868 PMID:28492532 PMID:33628209 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151806850 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598451 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:8401490


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126924711 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151808167 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:16199547 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13606878 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15108256 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15127297 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38467655 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127308108 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127308095 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15137263 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11075180 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10792291 PMID:21184155 PMID:25741868 PMID:28492532 PMID:28747913 PMID:9049783 PMID:9058718 PMID:9633906


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310494 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127317321 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127312903 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127302601 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15103210 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15154123 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629737 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127294223 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127309465 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15126022 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295829 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127308239 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127321956 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:25318403 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15167183 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15130995 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127305781 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127291111 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127286412 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14394868 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292755 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38481971 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151856105 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28359783 PMID:28492532 PMID:28747913


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15116613 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127292135 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15126486 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15155392 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15198502 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15126580 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127336286 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15167405 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14738274 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15138809 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26923439 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127337834 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26917888 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156054307 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15198428 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15197556 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127236156 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15127089 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13497484 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8561324 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:7860773


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15144179 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127320448 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15145462 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26898007 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127291098 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127268843 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127338237 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127316873 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127301430 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627010 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38492742 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127303278 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127295204 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127291852 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127230572 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151755954 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38498480 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26921399 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127277517 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127326631 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310799 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38499989 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38497167 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151802509 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Mashimo T, etal., PLoS One. 2010 Jan 25;5(1):e8870.
  • The annotation has been inferred from sequence orthology with Il2rg (Rattus norvegicus) [(IMP) inferred from mutant phenotype]
  • 16 additional annotations were made from Mashimo T, etal., PLoS One. 2010 Jan 25;5(1):e8870.
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127294173 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127310952 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127322453 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127232769 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151848771 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127315544 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127324908 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127330472 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127322763 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151765630 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38480374 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38470860 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127331009 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38470077 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38494777 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38487506 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127258053 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127231405 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598450 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:18941169 PMID:2984567


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598449 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:18941169


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8561323 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:8401490


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13606881 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602902 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13474817 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13606877 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598455 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:8900089


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602900 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:11129345 PMID:25326637 PMID:8557662 PMID:8961626


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598458 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:18728247 PMID:8900089


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598453 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:8401490


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598452 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:8401490


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13500916 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11522859 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602901 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38473256 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26904025 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38491772 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127238194 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11630926 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13465392 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26911202 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127264784 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15122866 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127255520 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127248663 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127250176 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127263600 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127275032 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127231764 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127241785 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127244186 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127273123 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127255971 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13813393 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13815064 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13473805 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150334420 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:25741868


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14735979 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14745367 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14690735 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14690739 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14718137 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14732565 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14730535 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613935 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15119424 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28875293 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627202 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11631755 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629288 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628763 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40906574 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150455175 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:25741868 PMID:28359783 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152123021 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152127718 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152090652 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152082390 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152167861 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152056289 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602899 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10444186 PMID:28492532 PMID:33628209 PMID:8961626


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152104145 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152033071 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152156824 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152120106 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13467990 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:8027558


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152161299 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152172487 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152035601 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152109564 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152037566 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152130336 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152067376 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152111833 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152055701 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152097191 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152159863 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152026437 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152064020 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152097885 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152092026 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152159938 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152050014 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152139531 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13606879 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152135898 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152069906 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152147094 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152109872 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152074631 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152161584 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152039064 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152080710 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152149762 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152158433 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152132294 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152120621 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13521524 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:11129345 PMID:12070011 PMID:23374275 PMID:7557965 PMID:8522327 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598457 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794431 PMID:16227049 PMID:20301584 PMID:23683512 PMID:25042067 PMID:25741868 PMID:28492532 PMID:29948574 PMID:31965297 PMID:7557965 PMID:7668284 PMID:9399950


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152983058 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13500277 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12742082 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:18615703


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40816201 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:14722921 PMID:18641513


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150435944 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:25741868


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38483311 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:16199547 PMID:28492532 PMID:28747913 PMID:29658452 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126760415 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126774562 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38483838 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:17576681 PMID:28492532 PMID:30850927 PMID:9536098


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598456 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:17576681 PMID:21184155 PMID:22039266 PMID:25741868 PMID:28492532 PMID:7557965 PMID:9058718 PMID:9150740 PMID:9536098


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151734701 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151738241 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151726133 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:18728247 PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150554377 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151755807 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:8299698


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14690729 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:11874464 PMID:16293754 PMID:28492532 PMID:28747913 PMID:8961626 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12894744 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:20301584 PMID:25741868 PMID:28492532 PMID:28747913 PMID:30622570 PMID:30778380 PMID:31799703 PMID:32499645


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151802459 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151739694 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151858567 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151799062 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151749195 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9058718 PMID:9536098


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151892794 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151860683 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151805238 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155268440 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150429575 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150547726 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794431 PMID:25741868 PMID:28492532 PMID:9633906


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155682960 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155682414 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155683027 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156450047 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155677852 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155682405 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155677803 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155678132 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151873282 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155675707 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127321952 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156219034 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155959043 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156005560 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156228833 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256651 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:21865537 PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155947588 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256657 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:26547715 PMID:28492532 PMID:32265911


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127238180 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:21184155 PMID:28492532 PMID:28747913 PMID:30622570 PMID:31799703


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13503563 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:28747913 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155960084 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:28747913 PMID:30622570 PMID:30778380 PMID:31799703 PMID:32499645


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156165985 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150429574 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602898 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:16199547 PMID:28359783 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156281424 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156197876 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12849773 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:8027558 PMID:9885222


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156237355 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151787497 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:9633906


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156252252 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156142692 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156013839 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126726879 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:33628209 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156255584 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156305725 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127243252 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:25843602 PMID:27484032 PMID:28492532 PMID:8605324


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156122102 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156093763 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38457340 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:19398866 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11075183 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:14966353 PMID:18641513 PMID:22039266 PMID:23683512 PMID:25741868 PMID:25869287 PMID:28492532 PMID:28747913 PMID:7632950 PMID:7668284 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11075187 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:11213805 PMID:16760466 PMID:17598841 PMID:21184155 PMID:22039266 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156131381 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127266280 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:16199547 PMID:28492532 PMID:33412294 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38484517 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794431 PMID:28492532 PMID:9633906


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151818362 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13802238 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:26525228 PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156126172 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127248386 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:16199547 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156184558 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:11260071 PMID:16199547 PMID:28492532 PMID:7557965 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156141669 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156184520 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:21732012 PMID:24612091 PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156185582 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156219963 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155968176 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:32888943


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156369002 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156343183 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256646 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:16199547 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151830906 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28109013 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12893765 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156121743 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156080958 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13467333 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:8299698


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155909777 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13807051 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:26547715 PMID:28492532 PMID:32265911


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156125247 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:28747913 PMID:30622570 PMID:30778380 PMID:31799703 PMID:32499645


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156108681 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151724835 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:21865537 PMID:28492532 PMID:31024866


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13499202 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28359783 PMID:28492532 PMID:28747913


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11634085 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:16199547 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156184593 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:32888943


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127248126 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151835799 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:27566612 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602903 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10784449 PMID:10794430 PMID:11213805 PMID:11961146 PMID:18641513 PMID:18941169 PMID:28492532 PMID:7557965 PMID:7668284 PMID:8027558 PMID:8298124 PMID:8462096 PMID:8712778 PMID:8781427 PMID:8961626 PMID:9058718 PMID:9150730


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155903471 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156345938 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21073741 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13606892 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156308643 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156036604 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155906985 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598454 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:12126929 PMID:28492532 PMID:7883965 PMID:7973658


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156238163 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13497665 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12849308 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:11129345 PMID:24534054 PMID:25741868 PMID:28492532 PMID:8088810


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156355975 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156142890 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156382767 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:28747913 PMID:30622570 PMID:30778380 PMID:31799703 PMID:32499645 PMID:33628209 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156408922 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:156177229 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150532652 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126725261 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:9633906


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127256136 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:10794430 PMID:16199547 PMID:28492532 PMID:9058718


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38488649 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:127251870 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532 PMID:28747913 PMID:8401490


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155950516 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking IL2RG and X-linked severe combined immunodeficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11559883 (Homo sapiens)
  • 8 RGD objects have been annotated to X-linked severe combined immunodeficiency  (DOID:0060013)
  • 11 papers in RGD have been used to annotate IL2RG
  • Curation Notes: ClinVar Annotator: match by term: X-linked severe combined immunodeficiency
  • Original References(s): PMID:11129345 PMID:28492532 PMID:8541866


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