AGT, angiotensinogen, 183

N. diseases: 765; N. variants: 43
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs699
rs699
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.100 0.950 20 1997 2016
dbSNP: rs4762
rs4762
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.050 0.800 5 1998 2013
dbSNP: rs762079672
rs762079672
0.882 0.040 1 230710211 missense variant C/T snv 4.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 1999 1999