rs3807306, IRF5

N. diseases: 8
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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 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
680 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
667 0.776 0.320 7 128940626 intron variant G/A;T snv 0.700 1.000 1 2012 2012
CATARACT, ANTERIOR POLAR
CUI: C1855179
Disease: CATARACT, ANTERIOR POLAR
27 0.776 0.320 7 128940626 intron variant G/A;T snv 0.010 1.000 1 2018 2018
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.776 0.320 7 128940626 intron variant G/A;T snv 0.010 1.000 1 2015 2015
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.776 0.320 7 128940626 intron variant G/A;T snv 0.010 1 2018 2018
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.776 0.320 7 128940626 intron variant G/A;T snv 0.010 1.000 1 2011 2011
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.776 0.320 7 128940626 intron variant G/A;T snv 0.010 1.000 1 2013 2013