rs1267969615, ACE

N. diseases: 100
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.
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 2000 2006
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 2000 2001
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 2007 2011
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 2013 2017
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 2012 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 2011 2011
Obesity
CUI: C0028754
Disease: Obesity
1111 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 2002 2012
Polycystic Kidney, Autosomal Dominant
CUI: C0085413
Disease: Polycystic Kidney, Autosomal Dominant
35 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 1997 2000
Vesicoureteral Reflux 1
CUI: C4551858
Disease: Vesicoureteral Reflux 1
10 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.020 1.000 2 2002 2009
ABLEPHARON-MACROSTOMIA SYNDROME
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
14 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2010 2010
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2005 2005
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2005 2005
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2018 2018
Aggressive periodontitis, generalized
CUI: C1719495
Disease: Aggressive periodontitis, generalized
16 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2009 2009
anaphylaxis
CUI: C0002792
Disease: anaphylaxis
4 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2010 2010
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2007 2007
Asthma
CUI: C0004096
Disease: Asthma
1536 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 1999 1999
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2007 2007
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2000 2000
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1 2008 2008
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2007 2007
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
24 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2017 2017
Cardiomyopathy, Hypertrophic, Familial
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
355 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1 1997 1997
Chronic glomerulonephritis
CUI: C0152451
Disease: Chronic glomerulonephritis
7 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2014 2014
Chronic Kidney Insufficiency
CUI: C0403447
Disease: Chronic Kidney Insufficiency
12 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2006 2006