Source: BEFREE

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: rs142677199
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 1999 1999
dbSNP: rs142677199
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 1999 1999
dbSNP: rs142677199
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 1999 1999
dbSNP: rs142677199
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 1999 1999