Source: ALL

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: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.100 0.842 38 1998 2020
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.100 0.947 19 1997 2017
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.040 1.000 4 2001 2020
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.040 1.000 4 2001 2020
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.030 1.000 3 2001 2008
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		0.030 1.000 3 2003 2014
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.030 1.000 3 2006 2009
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.020 0.500 2 2003 2003
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.020 1.000 2 2002 2006
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.020 1.000 2 2002 2007
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0085413
Disease: Polycystic Kidney, Autosomal Dominant
Polycystic Kidney, Autosomal Dominant 		0.020 1.000 2 2003 2003
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0265706
Disease: Gastroschisis
Gastroschisis 		0.020 1.000 2 2006 2018
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5 		0.020 0.500 2 2003 2003
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2017 2017
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension 		0.010 1.000 1 2009 2009
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0020544
Disease: Renal hypertension
Renal hypertension 		0.010 1.000 1 2002 2002
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined 		0.010 1.000 1 2001 2001
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0206586
Disease: Endolymphatic Hydrops
Endolymphatic Hydrops 		0.010 1.000 1 2008 2008
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2007 2007
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2007 2007
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0025281
Disease: Meniere Disease
Meniere Disease 		0.010 1.000 1 2008 2008
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0035078
Disease: Kidney Failure
Kidney Failure 		0.010 1.000 1 2006 2006
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		0.010 1.000 1 2020 2020
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2006 2006
dbSNP: rs4961
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		0.010 1.000 1 2006 2006