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.
ABLEPHARON-MACROSTOMIA SYNDROME
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
14 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2010 2010
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2005 2005
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2005 2005
Aggressive periodontitis, generalized
CUI: C1719495
Disease: Aggressive periodontitis, generalized
16 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2009 2009
anaphylaxis
CUI: C0002792
Disease: anaphylaxis
4 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2010 2010
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2019 2019
Angina, Unstable
CUI: C0002965
Disease: Angina, Unstable
21 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2006 2006
Asthma
CUI: C0004096
Disease: Asthma
1536 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 1999 1999
Atherosclerotic renal artery stenosis
CUI: C0340557
Disease: Atherosclerotic renal artery stenosis
4 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2006 2006
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2000 2000
Brain Infarction
CUI: C0751955
Disease: Brain Infarction
11 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2013 2013
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, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2007 2007
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
24 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2017 2017
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
Chronic glomerulonephritis
CUI: C0152451
Disease: Chronic glomerulonephritis
7 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2014 2014
Chronic heart failure
CUI: C0264716
Disease: Chronic heart failure
11 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2003 2003
Chronic Kidney Insufficiency
CUI: C0403447
Disease: Chronic Kidney Insufficiency
12 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2006 2006
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2005 2005
Coronary Stenosis
CUI: C0242231
Disease: Coronary Stenosis
20 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2011 2011
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
32 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2006 2006
Depressive Symptoms
CUI: C0086132
Disease: Depressive Symptoms
120 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2008 2008
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2000 2000
Disease of capillaries
CUI: C0155765
Disease: Disease of capillaries
5 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2011 2011
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
21 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2015 2015