rs4762, AGT

N. diseases: 35
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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.100 0.727 22 1994 2019
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.090 0.667 9 1994 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.050 0.600 5 1997 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.050 0.800 5 1998 2013
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.050 0.800 5 1996 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.040 0.750 4 1997 2017
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.030 0.667 3 1998 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.030 1.000 3 2009 2019
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.030 1.000 3 1996 2007
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.020 1.000 2 1999 2013
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.020 0.500 2 2011 2016
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.020 1.000 2 2011 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.020 1.000 2 1999 2015
ST segment elevation myocardial infarction
CUI: C1536220
Disease: ST segment elevation myocardial infarction
16 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.020 1.000 2 2011 2012
ST-segment elevation myocardial infarction (STEMI)
CUI: C4699152
Disease: ST-segment elevation myocardial infarction (STEMI)
2 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.020 0.500 2 2011 2012
Aortic Valve Stenosis
CUI: C0003507
Disease: Aortic Valve Stenosis
19 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1.000 1 1996 1996
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1 1997 1997
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1 1997 1997
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1 1997 1997
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1.000 1 2019 2019
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1 2001 2001
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1.000 1 2005 2005
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1.000 1 2007 2007
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1.000 1 2016 2016
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.010 1.000 1 1996 1996