rs4961, ADD1

N. diseases: 27
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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.100 0.842 38 1998 2020
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.100 0.947 19 1997 2017
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.040 1.000 4 2001 2020
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.040 1.000 4 2001 2020
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.030 1.000 3 2001 2008
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.030 1.000 3 2003 2014
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.030 1.000 3 2006 2009
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.020 1.000 2 2002 2006
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.020 0.500 2 2003 2003
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.020 1.000 2 2002 2007
Gastroschisis
CUI: C0265706
Disease: Gastroschisis
8 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.020 1.000 2 2006 2018
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.020 0.500 2 2003 2003
Polycystic Kidney, Autosomal Dominant
CUI: C0085413
Disease: Polycystic Kidney, Autosomal Dominant
35 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.020 1.000 2 2003 2003
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2006 2006
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2007 2007
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2007 2007
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2006 2006
Endolymphatic Hydrops
CUI: C0206586
Disease: Endolymphatic Hydrops
1 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2008 2008
Endothelial dysfunction
CUI: C0856169
Disease: Endothelial dysfunction
25 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2020 2020
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2001 2001
Hypernatremia
CUI: C0020488
Disease: Hypernatremia
3 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2008 2008
Kidney Failure
CUI: C0035078
Disease: Kidney Failure
36 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2006 2006
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2008 2008
Obesity
CUI: C0028754
Disease: Obesity
1111 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2017 2017
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2002 2002