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: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.800 0.900 20 1997 2018
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.100 0.865 89 1994 2019
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.100 0.795 39 1993 2014
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.100 0.905 21 1996 2018
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 0.950 20 1997 2016
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.100 0.850 20 1995 2016
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
Diabetes Mellitus, Non-Insulin-Dependent
0.100 0.933 15 1997 2017
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.100 1.000 15 1996 2014
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.100 0.857 14 1998 2019
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.100 0.818 11 1997 2015
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.100 1.000 11 1999 2016
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.090 0.778 9 1997 2015
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5
0.090 0.778 9 1997 2015
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension
0.090 0.889 9 1997 2012
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
Diabetes Mellitus, Insulin-Dependent
0.080 1.000 8 1996 2018
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0011847
Disease: Diabetes
Diabetes
0.070 0.714 7 1999 2014
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.070 0.714 7 1999 2014
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.060 1.000 6 2009 2019
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.060 1.000 6 1995 2019
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
0.060 1.000 6 1999 2007
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0013537
Disease: Eclampsia
Eclampsia
0.060 0.833 6 2003 2011
dbSNP: rs699
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.060 1.000 6 1999 2014