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.
High density lipoprotein measurement
867 0.821 0.071 15 58431476 intron variant C/G,T snp 0.30 0.32 0.800 3 2008 2016
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
923 0.821 0.071 15 58431476 intron variant C/G,T snp 0.30 0.32 0.800 3 2012 2017
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
814 0.821 0.071 15 58431476 intron variant C/G,T snp 0.30 0.32 0.800 2 2012 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.821 0.071 15 58431476 intron variant C/G,T snp 0.30 0.32 0.730 1.000 4 2008 2014
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
3393 0.821 0.071 15 58431476 intron variant C/G,T snp 0.30 0.32 0.700 1 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.821 0.071 15 58431476 intron variant C/G,T snp 0.30 0.32 0.040 1.000 4 2008 2014
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
189 0.821 0.071 15 58431476 intron variant C/G,T snp 0.30 0.32 0.030 1.000 3 2008 2014
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
24 0.821 0.071 15 58431476 intron variant C/G,T snp 0.30 0.32 0.010 1.000 1 2015 2015
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
41 0.821 0.071 15 58431476 intron variant C/G,T snp 0.30 0.32 0.010 1.000 1 2015 2015