rs1870634, None

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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 0.710 1.000 4 2015 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 0.700 1.000 1 2015 2015
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 0.010 1.000 1 2018 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 0.010 1.000 1 2018 2018