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 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.840 1.000 6 2011 2014
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.840 1.000 5 2008 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.730 1.000 4 2011 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
189 0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.030 1.000 3 2011 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1878 0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.010 1.000 1 2012 2012
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
48 0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.010 1 2012 2012
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
447 0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.010 1.000 1 2008 2008
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
121 0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.010 1 2012 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
131 0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.010 1 2012 2012
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
197 0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59 0.010 1.000 1 2012 2012