rs1333047, CDKN2B-AS1

N. diseases: 9
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.
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.700 1.000 2 2011 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.700 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.700 1.000 1 2018 2018
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2013 2013
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2013 2013
Arteriosclerotic cardiovascular disease, NOS
CUI: C3665365
Disease: Arteriosclerotic cardiovascular disease, NOS
5 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2018 2018
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2018 2018
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2018 2018
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2015 2015