rs1411224107, SERPINE1

N. diseases: 4
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.
Arteriosclerosis Obliterans
CUI: C0003851
Disease: Arteriosclerosis Obliterans
2 0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06 0.010 1.000 1 2000 2000
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06 0.010 1.000 1 2000 2000
Factor XII Deficiency
CUI: C0015526
Disease: Factor XII Deficiency
13 0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06 0.010 1 2007 2007
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.882 0.160 7 101128439 missense variant C/T snv 7.0E-06 0.010 1 2007 2007