rs2453021, TNFRSF9

N. diseases: 6
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.
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.807 0.080 1 7929506 intron variant C/A;T snv 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.807 0.080 1 7929506 intron variant C/A;T snv 0.010 1.000 1 2014 2014
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.807 0.080 1 7929506 intron variant C/A;T snv 0.010 1 2014 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.080 1 7929506 intron variant C/A;T snv 0.010 1 2014 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.807 0.080 1 7929506 intron variant C/A;T snv 0.010 1 2014 2014
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.807 0.080 1 7929506 intron variant C/A;T snv 0.010 1 2014 2014