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: rs1063192
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		0.810 1.000 2 2012 2012
dbSNP: rs1063192
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0017638
Disease: Glioma
Glioma 		0.710 1.000 2 2009 2018
dbSNP: rs2069416
rs2069416
CDKN2B ; CDKN2B-AS1
0.925 0.040 9 22010005 intron variant T/A;G snv
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: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 2 2011 2013
dbSNP: rs1063192
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2011 2011
dbSNP: rs1063192
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv
CUI: C0017601
Disease: Glaucoma
Glaucoma 		0.710 1.000 1 2011 2017
dbSNP: rs2069416
rs2069416
CDKN2B ; CDKN2B-AS1
0.925 0.040 9 22010005 intron variant T/A;G snv
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		0.700 1.000 1 2012 2012
dbSNP: rs2069418
rs2069418
CDKN2B ; CDKN2B-AS1
1.000 0.040 9 22009699 intron variant G/C snv 0.70
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2011 2011
dbSNP: rs2069418
rs2069418
CDKN2B ; CDKN2B-AS1
1.000 0.040 9 22009699 intron variant G/C snv 0.70
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: 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: 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: 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: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2014 2014
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: rs545226
rs545226
CDKN2B-AS1 ; UBA52P6
1.000 0.040 9 22012423 non coding transcript exon variant G/A snv 0.68
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		0.700 1.000 1 2012 2012
dbSNP: rs1333049
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.900 1.000 9 2007 2020
dbSNP: rs4977574
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.840 1.000 5 2011 2018
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 3 2008 2016
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 3 2011 2013
dbSNP: rs1333042
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.820 1.000 3 2011 2016
dbSNP: rs1412829
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28
CUI: C0017638
Disease: Glioma
Glioma 		0.810 1.000 3 2009 2016
dbSNP: rs1537370
rs1537370
CDKN2B-AS1
1.000 9 22084311 intron variant C/T snv 0.55
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.800 1.000 3 2011 2013
dbSNP: rs2891168
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 3 2011 2013
dbSNP: rs4977756
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C0017638
Disease: Glioma
Glioma 		0.900 0.875 3 2009 2020
dbSNP: rs944797
rs944797
CDKN2B-AS1
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 3 2011 2013