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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.925 0.040 2 187478770 missense variant T/C;G snv 0.29 0.010 1.000 1 2017 2017
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.925 0.040 2 187478770 missense variant T/C;G snv 0.29 0.010 1.000 1 2009 2009