rs640198, MMP13

N. diseases: 4
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 Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.851 0.040 11 102954362 intron variant T/G snv 0.68 0.010 1.000 1 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.040 11 102954362 intron variant T/G snv 0.68 0.010 1.000 1 2012 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.040 11 102954362 intron variant T/G snv 0.68 0.010 1.000 1 2012 2012
Triple vessel disease
CUI: C0856738
Disease: Triple vessel disease
3 0.851 0.040 11 102954362 intron variant T/G snv 0.68 0.010 1.000 1 2012 2012