rs699, AGT

N. diseases: 134
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.
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 2 1997 1999
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 2 2008 2015
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 2 2001 2003
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 2 2008 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1 2008 2008
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1 1997 1997
Hypotension, Orthostatic
CUI: C0020651
Disease: Hypotension, Orthostatic
21 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1 2002 2002
Left ventricular dilatation
CUI: C0344911
Disease: Left ventricular dilatation
3 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1 1996 1996
Lupus Nephritis
CUI: C0024143
Disease: Lupus Nephritis
64 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1 2005 2005
ST-segment elevation myocardial infarction (STEMI)
CUI: C4699152
Disease: ST-segment elevation myocardial infarction (STEMI)
2 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1 2011 2011
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.030 0.333 3 2001 2011
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 0.500 2 1997 2007
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 0.500 2 2006 2013
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.070 0.714 7 1999 2014
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.070 0.714 7 1999 2014
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.040 0.750 4 2011 2018
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.040 0.750 4 1995 2007
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.090 0.778 9 1997 2015
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.090 0.778 9 1997 2015
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.100 0.795 39 1993 2014
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.100 0.818 11 1997 2015
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.060 0.833 6 2003 2011
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.100 0.850 20 1995 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.100 0.857 14 1998 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.100 0.865 89 1994 2019