rs387907201, F2

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.
THROMBOPHILIA DUE TO THROMBIN DEFECT
CUI: C3160733
Disease: THROMBOPHILIA DUE TO THROMBIN DEFECT
2 1.000 0.080 11 46739326 missense variant G/A;T snv 0.700 0
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 1.000 0.080 11 46739326 missense variant G/A;T snv 0.020 1.000 2 2016 2018
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
31 1.000 0.080 11 46739326 missense variant G/A;T snv 0.010 1.000 1 2018 2018
Hereditary factor II deficiency disease
CUI: C0272317
Disease: Hereditary factor II deficiency disease
14 1.000 0.080 11 46739326 missense variant G/A;T snv 0.010 1.000 1 2018 2018