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: rs10811656
rs10811656
0.807 0.200 9 22124473 intron variant C/T snv 0.47
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 1 2013 2013
dbSNP: rs10811656
rs10811656
0.807 0.200 9 22124473 intron variant C/T snv 0.47
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 1.000 2 2011 2016
dbSNP: rs10811656
rs10811656
0.807 0.200 9 22124473 intron variant C/T snv 0.47
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.020 1.000 2 2013 2016
dbSNP: rs10811656
rs10811656
0.807 0.200 9 22124473 intron variant C/T snv 0.47
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2016 2016
dbSNP: rs10811656
rs10811656
0.807 0.200 9 22124473 intron variant C/T snv 0.47
CUI: C0340288
Disease: Stable angina
Stable angina
0.010 1.000 1 2016 2016
dbSNP: rs10811656
rs10811656
0.807 0.200 9 22124473 intron variant C/T snv 0.47
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.010 1.000 1 2013 2013
dbSNP: rs10811656
rs10811656
0.807 0.200 9 22124473 intron variant C/T snv 0.47
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2016 2016