rs1799752, ACE

N. diseases: 11
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.
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
110 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.020 1.000 2 2007 2010
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1062 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.010 1.000 1 2016 2016
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
66 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.010 1.000 1 2014 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
197 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.010 1.000 1 2009 2009
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
65 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.010 1.000 1 2014 2014
Heart failure
CUI: C0018801
Disease: Heart failure
91 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.010 1.000 1 2014 2014
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
209 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.010 1.000 1 2011 2011
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
93 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.010 1.000 1 2010 2010
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
95 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.010 1.000 1 2013 2013
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
100 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.010 1.000 1 2013 2013
Neonatal Drug Withdrawal
CUI: C3540839
Disease: Neonatal Drug Withdrawal
3 0.756 0.286 17 63488529 intron variant T/TATACAGTCACTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCC,TG in-del 0.010 1.000 1 2010 2010