Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
Familial hypercholesterolemia - heterozygous
0.010 1.000 1 2000 2000
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C1970945
Disease: MAJOR AFFECTIVE DISORDER 6
MAJOR AFFECTIVE DISORDER 6
0.010 1.000 1 2000 2000
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C1852197
Disease: MAJOR AFFECTIVE DISORDER 1
MAJOR AFFECTIVE DISORDER 1
0.010 1.000 1 2000 2000
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.010 1.000 1 2000 2000
dbSNP: rs887280103
rs887280103
ACE
1.000 0.120 17 63477294 missense variant C/G snv 1.4E-05
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 1.000 1 2000 2000
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.020 1.000 2 2000 2001
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C1096293
Disease: Macroangiopathy
Macroangiopathy
0.010 1.000 1 2001 2001
dbSNP: rs1415088003
rs1415088003
ACE
0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
0.010 1.000 1 2001 2001
dbSNP: rs145579007
rs145579007
ACE
0.925 0.080 17 63496503 missense variant G/A snv 1.0E-04 1.0E-04
CUI: C0038443
Disease: Stress, Psychological
Stress, Psychological
0.010 1.000 1 2001 2001
dbSNP: rs750712925
rs750712925
ACE
0.925 0.080 17 63477227 missense variant G/A;C;T snv 3.2E-05
CUI: C0038443
Disease: Stress, Psychological
Stress, Psychological
0.010 1.000 1 2001 2001
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0020651
Disease: Hypotension, Orthostatic
Hypotension, Orthostatic
0.010 < 0.001 1 2002 2002
dbSNP: rs1334067073
rs1334067073
ACE
0.925 0.120 17 63478025 missense variant C/G;T snv 4.2E-06
CUI: C0020544
Disease: Renal hypertension
Renal hypertension
0.010 1.000 1 2002 2002
dbSNP: rs1415088003
rs1415088003
ACE
0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
0.010 1.000 1 2002 2002
dbSNP: rs1415088003
rs1415088003
ACE
0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 1.000 1 2002 2002
dbSNP: rs759009903
rs759009903
ACE
17 63484413 missense variant C/G;T snv 1.6E-05
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.010 1.000 1 2002 2002
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
0.050 1.000 5 1999 2003
dbSNP: rs1157043147
rs1157043147
ACE
1.000 0.120 17 63477150 missense variant T/C snv 2.8E-05
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 1.000 1 2003 2003
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0018799
Disease: Heart Diseases
Heart Diseases
0.010 1.000 1 2003 2003
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0152025
Disease: Polyneuropathy
Polyneuropathy
0.010 1.000 1 2003 2003
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0035078
Disease: Kidney Failure
Kidney Failure
0.010 1.000 1 2003 2003
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis
0.010 1.000 1 2003 2003
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency
0.010 1.000 1 2003 2003
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0085096
Disease: Peripheral Vascular Diseases
Peripheral Vascular Diseases
0.010 1.000 1 2003 2003
dbSNP: rs867394500
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv
CUI: C0035078
Disease: Kidney Failure
Kidney Failure
0.010 1.000 1 2003 2003
dbSNP: rs867394500
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency
0.010 1.000 1 2003 2003