Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs974819
rs974819 		0.807 0.080 11 103789839 intron variant T/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.820 1.000 4 2012 2018
dbSNP: rs974819
rs974819 		0.807 0.080 11 103789839 intron variant T/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.810 1.000 2 2011 2012
dbSNP: rs974819
rs974819 		0.807 0.080 11 103789839 intron variant T/A;C snv
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0.700 1.000 1 2013 2013
dbSNP: rs974819
rs974819 		0.807 0.080 11 103789839 intron variant T/A;C snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2014 2014
dbSNP: rs974819
rs974819 		0.807 0.080 11 103789839 intron variant T/A;C snv
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2014 2014
dbSNP: rs974819
rs974819 		0.807 0.080 11 103789839 intron variant T/A;C snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2012 2012