rs17231896, CETP

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.
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.925 0.120 16 56982180 missense variant G/A;C snv 0.010 1.000 1 2017 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.120 16 56982180 missense variant G/A;C snv 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.925 0.120 16 56982180 missense variant G/A;C snv 0.010 1.000 1 2017 2017