rs891512, NOS3

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 0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 0.010 1.000 1 2017 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 0.010 1.000 1 2020 2020
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 0.010 1.000 1 2018 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 0.010 1.000 1 2012 2012