rs3789683, F3

N. diseases: 3
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.
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.925 0.200 1 94530506 missense variant C/T snv 6.5E-03 1.0E-02 0.020 1.000 2 2015 2017
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.925 0.200 1 94530506 missense variant C/T snv 6.5E-03 1.0E-02 0.010 1.000 1 2015 2015
Factor V Leiden mutation
CUI: C0584960
Disease: Factor V Leiden mutation
46 0.925 0.200 1 94530506 missense variant C/T snv 6.5E-03 1.0E-02 0.010 1.000 1 2015 2015