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: rs4762
rs4762
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2005 2005
dbSNP: rs56073403
rs56073403
0.882 0.160 1 230710009 missense variant T/C snv 7.2E-04 6.8E-04
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2005 2005
dbSNP: rs699
rs699
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2005 2005