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.
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 1995 1995
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
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
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
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
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
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
Renal Artery Stenosis
CUI: C0035067
Disease: Renal Artery Stenosis
8 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 1999 1999
Right Ventricular Hypertrophy
CUI: C0162770
Disease: Right Ventricular Hypertrophy
6 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 1999 1999
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
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
Familial hypercholesterolemia - heterozygous
CUI: C0342882
Disease: 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
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
MAJOR AFFECTIVE DISORDER 1
CUI: C1852197
Disease: MAJOR AFFECTIVE DISORDER 1
34 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2000 2000
MAJOR AFFECTIVE DISORDER 2
CUI: C1839839
Disease: MAJOR AFFECTIVE DISORDER 2
34 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2000 2000
MAJOR AFFECTIVE DISORDER 4
CUI: C1970943
Disease: MAJOR AFFECTIVE DISORDER 4
34 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2000 2000
MAJOR AFFECTIVE DISORDER 6
CUI: C1970945
Disease: MAJOR AFFECTIVE DISORDER 6
34 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2000 2000
Tonsillitis
CUI: C0040425
Disease: Tonsillitis
9 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2000 2000
Macroangiopathy
CUI: C1096293
Disease: Macroangiopathy
6 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2001 2001
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
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
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
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
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
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