rs974819, None

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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.080 11 103789839 intron variant T/A;C snv 0.820 1.000 4 2012 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.807 0.080 11 103789839 intron variant T/A;C snv 0.810 1.000 2 2011 2012
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.807 0.080 11 103789839 intron variant T/A;C snv 0.700 1.000 1 2013 2013
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.807 0.080 11 103789839 intron variant T/A;C snv 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.807 0.080 11 103789839 intron variant T/A;C snv 0.010 1.000 1 2014 2014
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.807 0.080 11 103789839 intron variant T/A;C snv 0.010 1.000 1 2012 2012