rs1800595, F5

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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.925 0.080 1 169541110 missense variant T/C;G snv 5.7E-02 0.010 1.000 1 2017 2017
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.925 0.080 1 169541110 missense variant T/C;G snv 5.7E-02 0.010 1.000 1 2012 2012