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.
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
Erythrocytosis due to low atmospheric pressure
13 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2017 2017
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 1999 1999
Familial hypercholesterolemia - heterozygous
34 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2000 2000
Focal glomerulosclerosis
CUI: C0017668
Disease: Focal glomerulosclerosis
50 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2003 2003
Heart Diseases
CUI: C0018799
Disease: Heart Diseases
45 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2003 2003
Heart Failure, Systolic
CUI: C1135191
Disease: Heart Failure, Systolic
6 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 1999 1999
Henoch-Schonlein purpura nephritis
CUI: C2721603
Disease: Henoch-Schonlein purpura nephritis
6 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2015 2015
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2009 2009
High altitude pulmonary edema
CUI: C0340100
Disease: High altitude pulmonary edema
45 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2011 2011
Hyperaldosteronism
CUI: C0020428
Disease: Hyperaldosteronism
6 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2015 2015
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2008 2008
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
64 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2006 2006
Hypertension, Renovascular
CUI: C0020545
Disease: Hypertension, Renovascular
8 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2004 2004
hypertensive nephropathy
CUI: C0848548
Disease: hypertensive nephropathy
8 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2010 2010
Hypertrophic obstructive cardiomyopathy
90 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2011 2011
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
Infarction, Lacunar
CUI: C0333559
Disease: Infarction, Lacunar
18 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2000 2000
Isolated systolic hypertension
CUI: C0745133
Disease: Isolated systolic hypertension
3 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2002 2002
Isovaleryl-CoA dehydrogenase deficiency
55 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2010 2010
Kidney Failure
CUI: C0035078
Disease: Kidney Failure
36 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2003 2003
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
Left ventricular systolic dysfunction
11 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2015 2015