Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs891512
rs891512
NOS3
0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2020 2020
dbSNP: rs891512
rs891512
NOS3
0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2018 2018
dbSNP: rs891512
rs891512
NOS3
0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2012 2012
dbSNP: rs891512
rs891512
NOS3
0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2017 2017