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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.820 1.000 5 2011 2014
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.800 1 2009 2009
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.730 1.000 4 2012 2015
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
331 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.710 1.000 2 2014 2014
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
814 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.700 1 2013 2013
Low density lipoprotein cholesterol measurement
676 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.700 1 2013 2013
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
189 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.010 1.000 1 2012 2012
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
209 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
131 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.010 1.000 1 2014 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
197 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.010 1.000 1 2015 2015
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
32 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.010 1.000 1 2015 2015
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
57 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.010 1.000 1 2012 2012
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
121 0.784 0.071 19 11052925 intron variant G/T snp 0.18 0.010 1.000 1 2014 2014