rs10118757, MTAP

N. diseases: 7
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 Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.020 1.000 2 2012 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.010 1.000 1 2009 2009
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.010 1.000 1 2013 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.010 1.000 1 2013 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.010 1.000 1 2009 2009
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.010 1.000 1 2009 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.010 1 2013 2013