IRF5, interferon regulatory factor 5, 3663

N. diseases: 226; N. variants: 15
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3823536
rs3823536
Entrez Id: 3663
Gene Symbol: IRF5
IRF5
CUI: C1527336
Disease:
Sjogren's Syndrome
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899 2017
dbSNP: rs3757387
rs3757387
Entrez Id: 3663
Gene Symbol: IRF5
IRF5
CUI: C1527336
Disease:
Sjogren's Syndrome
C 0.700 GeneticVariation GWASCAT Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome. 24097067 2013