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GENE - TERM ANNOTATION REPORT

366 Annotations Found.

An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Kiyozumi D, etal., Biochem Biophys Res Commun. 2011 Jul 29;411(2):440-4. doi: 10.1016/j.bbrc.2011.06.174. Epub 2011 Jul 2.
  • The annotation has been inferred from sequence orthology with Frem2 (Rattus norvegicus) [(IAGP) inferred by association of genotype and phenotype]
  • 12 additional annotations were made from Kiyozumi D, etal., Biochem Biophys Res Commun. 2011 Jul 29;411(2):440-4. doi: 10.1016/j.bbrc.2011.06.174. Epub 2011 Jul 2.
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15109004 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11607693 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151732783 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:30773290


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868810 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910969 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619850 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8556569 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:18203166


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13534437 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13534436 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:40888515 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13704830 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14399446 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:29688405


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15104405 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8595577 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:15838507 PMID:18671281 PMID:29688405


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11640966 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:29688405 PMID:30802441


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603165 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869157 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15112446 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911506 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911507 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14693056 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868430 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14693057 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28872024 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15110234 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867441 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911594 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612298 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871131 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613589 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624282 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868295 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911545 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871292 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911679 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911681 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11601829 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602748 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617632 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11659867 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11608100 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11606782 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11655452 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618548 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911012 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618172 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910965 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11609356 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911733 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867742 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911631 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911632 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599585 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911634 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11605395 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11610618 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11604324 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612905 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911053 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652292 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868156 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11660364 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613387 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600204 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15192338 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911055 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615896 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868677 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614867 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871134 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622454 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911142 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613554 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11657426 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645114 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869029 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612914 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11611890 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867436 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871620 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15113102 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28872014 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622150 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612954 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11662066 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650024 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911143 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28870607 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11601070 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867748 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871618 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613432 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617472 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11609971 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911680 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621126 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911189 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871623 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618481 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622339 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911191 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911195 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615312 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11609573 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650998 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28872236 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911054 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617774 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617209 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618848 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28872232 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621667 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624879 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911732 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28870794 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15141529 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622119 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911193 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28872018 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615268 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11648487 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11636363 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599779 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869162 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617228 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11643748 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647506 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600970 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11601568 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911190 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620624 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871809 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613085 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614354 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652604 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617001 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623974 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622921 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625531 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11608509 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28872228 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868676 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623141 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869159 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618110 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649504 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11657404 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28872021 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868814 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11606296 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911544 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619285 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910968 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910967 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11578418 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11607541 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11651778 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615873 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621563 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617490 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871615 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620883 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600491 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623027 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619019 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11611199 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622310 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11655316 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11605671 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910852 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11611215 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11662376 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624415 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11661740 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911305 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11661298 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869031 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911194 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911359 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911361 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15141272 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652735 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11350583 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624574 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911251 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867740 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911505 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28873727 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15137269 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602832 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15111702 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867578 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645412 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11662143 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622622 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619506 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11579210 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911360 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10048326 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868 PMID:26275891 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10049623 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624366 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868578 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11656296 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911304 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624850 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602981 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28870957 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11350814 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11660950 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625679 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911633 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621312 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624585 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626105 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11605498 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626165 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622741 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10050122 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11609800 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10049630 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626132 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15164262 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911250 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620389 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621234 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15138269 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11605196 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599013 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869316 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15150709 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653377 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624261 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623508 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619728 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869161 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625678 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11600982 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625690 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871812 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867745 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28869312 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624151 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910854 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625575 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911783 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11350836 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911303 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911192 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11663857 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11656318 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11657163 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620720 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11603638 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11625459 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13515847 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620049 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10047606 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10047611 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617458 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613927 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11545212 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11616894 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615748 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11549338 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911456 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624924 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871480 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10047608 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624878 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618635 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621176 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10047609 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11611679 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11611935 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623378 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621538 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11624006 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619238 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911593 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11542841 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10047610 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10047612 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34889446 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34889449 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34889412 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620333 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34889415 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612435 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618854 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15112828 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623731 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: FRASER SYNDROME 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15104941 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:150436085 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126741209 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152999473 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10049626 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614469 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10049625 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620157 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11581526 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15135354 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10049627 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10049628 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617912 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910906 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11634295 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30143558


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151727665 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151732788 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:30773290


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621433 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11602637 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868297 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11599800 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620162 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619751 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11577713 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615513 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10047607 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868155 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910907 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871477 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613384 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13833682 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11601866 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11638137 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620371 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622432 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11610113 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11604645 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11606276 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871129 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868293 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868579 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11611276 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151662001 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28910966 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11607205 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868811 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622760 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28871290 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15132762 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13518315 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11611181 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911013 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618496 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615860 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:152999320 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613844 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911011 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28870604 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28868573 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911091 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28870956 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11633259 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29618029 PMID:30838450


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28911546 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614829 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11622975 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867438 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:24115501 PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28873730 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867434 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614548 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13214978 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:24700879 PMID:25741868 PMID:28492532 PMID:30143558


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867582 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28867587 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


    • An association has been curated linking FREM2 and Fraser syndrome 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11623086 (Homo sapiens)
  • 1 RGD objects have been annotated to Fraser syndrome 2  (DOID:0111407)
  • 5 papers in RGD have been used to annotate FREM2
  • Curation Notes: ClinVar Annotator: match by term: Fraser syndrome 2
  • Original References(s): PMID:28492532


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