Source: GWASDB

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: rs3217992
rs3217992
CDKN2B ; CDKN2B-AS1
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 2 2011 2013
dbSNP: rs3217992
rs3217992
CDKN2B ; CDKN2B-AS1
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32
CUI: C0017638
Disease: Glioma
Glioma 		0.700 1.000 1 2011 2011
dbSNP: rs3217992
rs3217992
CDKN2B ; CDKN2B-AS1
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		0.700 1.000 1 2012 2012
dbSNP: rs3217992
rs3217992
CDKN2B ; CDKN2B-AS1
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0.700 1.000 1 2013 2013
dbSNP: rs3217992
rs3217992
CDKN2B ; CDKN2B-AS1
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32
CUI: C0017601
Disease: Glaucoma
Glaucoma 		0.700 1.000 1 2012 2012
dbSNP: rs3217992
rs3217992
CDKN2B ; CDKN2B-AS1
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2014 2014