rs3807306, IRF5

N. diseases: 3
Source: GWASDB ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1613 0.776 0.320 7 128940626 intron variant G/A;T snv 0.800 1.000 2 2011 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
94 0.776 0.320 7 128940626 intron variant G/A;T snv 0.700 1.000 1 2011 2011
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
561 0.776 0.320 7 128940626 intron variant G/A;T snv 0.700 1.000 1 2012 2012