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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05 0.830 1.000 5 2007 2015
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05 0.820 1.000 8 2011 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05 0.720 1.000 4 2013 2018
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
3393 0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05 0.700 2 2012 2013
Glaucoma
CUI: C0017601
Disease: Glaucoma
209 0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05 0.700 1 2012 2012
Malignant Central Nervous System Neoplasm
87 0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05 0.700 1 2011 2011
Aspartate aminotransferase measurement
108 0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05 0.700 1 2011 2011
Unipolar Depression
CUI: C0041696
Disease: Unipolar Depression
378 0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05 0.700 1 2013 2013
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
91 0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05 0.010 1.000 1 2015 2015
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
189 0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05 0.010 1.000 1 2015 2015