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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.878 0.036 6 12927312 intron variant C/G snp 0.25 0.820 1.000 4 2011 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 0.878 0.036 6 12927312 intron variant C/G snp 0.25 0.820 1.000 3 2009 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.878 0.036 6 12927312 intron variant C/G snp 0.25 0.020 1.000 2 2013 2015