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: rs1042309696
rs1042309696
ACE
17 63487006 synonymous variant T/C snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2008 2008
dbSNP: rs1042309696
rs1042309696
ACE
17 63487006 synonymous variant T/C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2008 2008
dbSNP: rs1156835126
rs1156835126
ACE
17 63477230 missense variant G/A snv 4.2E-05
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2010 2010
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: rs1181835738
rs1181835738
ACE
17 63490971 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.010 1.000 1 2009 2009
dbSNP: rs1205538057
rs1205538057
ACE
0.827 0.200 17 63483937 missense variant A/G snv 4.0E-06
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2012 2012
dbSNP: rs1205538057
rs1205538057
ACE
0.827 0.200 17 63483937 missense variant A/G snv 4.0E-06
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.010 1.000 1 2008 2008
dbSNP: rs1205538057
rs1205538057
ACE
0.827 0.200 17 63483937 missense variant A/G snv 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2012 2012
dbSNP: rs1205538057
rs1205538057
ACE
0.827 0.200 17 63483937 missense variant A/G snv 4.0E-06
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.010 1.000 1 2019 2019
dbSNP: rs121912703
rs121912703
ACE
17 63496977 missense variant C/T snv 3.7E-05 4.9E-05
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		0.010 1.000 1 2006 2006
dbSNP: rs1221928144
rs1221928144
ACE
1.000 0.040 17 63477950 missense variant G/A;C snv 8.2E-06
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.010 1.000 1 2007 2007
dbSNP: rs1241356540
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 < 0.001 1 2006 2006
dbSNP: rs1241356540
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2006 2006
dbSNP: rs1241356540
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.010 < 0.001 1 2006 2006
dbSNP: rs1241356540
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv
CUI: C0730285
Disease: Diabetic macular edema
Diabetic macular edema 		0.010 < 0.001 1 2006 2006
dbSNP: rs1241356540
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 < 0.001 1 2006 2006
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2018 2018
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0024143
Disease: Lupus Nephritis
Lupus Nephritis 		0.010 < 0.001 1 2005 2005
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2011 2011
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0340100
Disease: High altitude pulmonary edema
High altitude pulmonary edema 		0.010 1.000 1 2011 2011
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		0.010 1.000 1 2005 2005
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0029899
Disease: Otosclerosis
Otosclerosis 		0.010 1.000 1 2008 2008
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.010 1.000 1 2004 2004
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0344911
Disease: Left ventricular dilatation
Left ventricular dilatation 		0.010 < 0.001 1 1996 1996
dbSNP: rs1267969615
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06
CUI: C0152451
Disease: Chronic glomerulonephritis
Chronic glomerulonephritis 		0.010 1.000 1 2014 2014