rs142846443, PROS1

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.
Plasminogen Deficiency, Type I
CUI: C1968804
Disease: Plasminogen Deficiency, Type I
13 1.000 0.120 3 93877074 missense variant T/C snv 8.0E-04 4.3E-04 0.010 1.000 1 2017 2017
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 1.000 0.120 3 93877074 missense variant T/C snv 8.0E-04 4.3E-04 0.010 1.000 1 2017 2017