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.
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.050 1.000 5 2004 2015
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 Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.040 1.000 4 2000 2019
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.040 1.000 4 1999 2014
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.030 1.000 3 2011 2017
Maternal hypertension
CUI: C0565599
Disease: Maternal hypertension
22 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.030 1.000 3 1999 2004
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
Obesity
CUI: C0028754
Disease: Obesity
1111 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.030 1.000 3 2002 2012
Polycystic Kidney, Autosomal Dominant
CUI: C0085413
Disease: Polycystic Kidney, Autosomal Dominant
35 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.030 1.000 3 1997 2003
Acromegaly
CUI: C0001206
Disease: Acromegaly
25 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2011 2017
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 1999 2007
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 1999 2007
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2011 2011
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
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
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2001 2007
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2012 2020
genetic hypertension
CUI: C0598428
Disease: genetic hypertension
2 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 1995 2012
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2011 2011
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
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2009 2015
Mitral Valve Prolapse Syndrome
CUI: C0026267
Disease: Mitral Valve Prolapse Syndrome
29 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2008 2008
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