rs751141, EPHX2

N. diseases: 9
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.
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1189 0.784 0.179 8 27516348 missense variant G/A snp 0.12 0.11 0.700 6 2000 2005
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
209 0.784 0.179 8 27516348 missense variant G/A snp 0.12 0.11 0.030 1.000 3 2008 2010
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.784 0.179 8 27516348 missense variant G/A snp 0.12 0.11 0.020 0.500 2 2010 2011
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
216 0.784 0.179 8 27516348 missense variant G/A snp 0.12 0.11 0.010 1.000 1 2014 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
197 0.784 0.179 8 27516348 missense variant G/A snp 0.12 0.11 0.010 1 2011 2011
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
331 0.784 0.179 8 27516348 missense variant G/A snp 0.12 0.11 0.010 1.000 1 2010 2010
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
189 0.784 0.179 8 27516348 missense variant G/A snp 0.12 0.11 0.010 1.000 1 2010 2010
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.784 0.179 8 27516348 missense variant G/A snp 0.12 0.11 0.010 1.000 1 2010 2010
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
44 0.784 0.179 8 27516348 missense variant G/A snp 0.12 0.11 0.010 1.000 1 2010 2010