rs7071489 Rat Genome Database

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Variant: rs7071489 -  Homo sapiens

RGD ID: 406290061
RS ID: rs7071489
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: ?
Position
Assembly Chr Position
GRCh38 10 131,614,647
JBrowse: View Region in Genome Browser (JBrowse)
Model



Experimental Factor Annotations    Click to see Annotation Detail View
Object SymbolSpeciesTermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
rs7071489Humansuberic acid measurement  IAGP 405850206 GWAS_CATALOGPMID:23823483
GWAS QTLs Related by Peak Marker
Data has come from the GWAS Catalog   
QTL GWAS Catalog Study Disease Trait Study Size Risk Allele Risk Allele Frequency P Value P Value MLOG Peak Marker Reported Odds Ratio or Beta-coefficient Ontology Accession PubMed
GWAS625995_H GCST009391 Metabolite levels 2,076 European ancestry individuals ? NR 0.000004 5.398 rs7071489 0.29580685 suberic acid measurement (EFO:0010534)
PMID:23823483

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
GWAS Catalog GCST009391 GWAS Catalog