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.
Factor XII Deficiency
CUI: C0015526
Disease: Factor XII Deficiency
13 1.000 0.080 5 177404082 missense variant C/G snv 3.1E-03 1.1E-03 0.700 1.000 1 2011 2011
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 1.000 0.080 5 177404082 missense variant C/G snv 3.1E-03 1.1E-03 0.010 1.000 1 2018 2018