rs3823536, IRF5

N. diseases: 2
Source: ALL
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.
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.925 0.280 7 128939612 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.925 0.280 7 128939612 intron variant G/A snv 0.40 0.700 1.000 1 2017 2017