Source: GWASCAT

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: 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 5 2007 2020
dbSNP: rs1333049
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.900 0.944 2 2007 2019
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 2 2009 2020
dbSNP: rs10757274
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.900 1.000 1 2008 2016
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.900 0.923 1 2007 2019
dbSNP: rs4977574
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.890 1.000 2 2007 2019
dbSNP: rs4977574
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.880 1.000 1 2007 2018
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 3 2011 2018
dbSNP: rs1333040
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.840 1.000 2 2008 2015
dbSNP: rs2891168
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.820 1.000 3 2007 2018
dbSNP: rs2157719
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71
CUI: C0017638
Disease: Glioma
Glioma 		0.820 1.000 2 2009 2019
dbSNP: rs10757272
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.820 1.000 1 2012 2019
dbSNP: rs10965235
rs10965235
CDKN2B-AS1
1.000 0.040 9 22115106 intron variant C/A snv 0.15
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.820 1.000 1 2010 2014
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 1 2011 2016
dbSNP: rs7865618
rs7865618
CDKN2B-AS1
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.820 1.000 1 2011 2017
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 1 2012 2012
dbSNP: rs10738607
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.810 1.000 1 2007 2018
dbSNP: rs1333042
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.810 1.000 1 2007 2018
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 1 2009 2016
dbSNP: rs4977756
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		0.810 1.000 1 2011 2014
dbSNP: rs523096
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30
CUI: C0017601
Disease: Glaucoma
Glaucoma 		0.810 1.000 1 2012 2012
dbSNP: rs564398
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.810 1.000 1 2007 2012
dbSNP: rs6475606
rs6475606
CDKN2B-AS1
0.882 0.080 9 22081851 intron variant C/T snv 0.62
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.810 1.000 1 2012 2012
dbSNP: rs2157719
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		0.800 1.000 2 2012 2015
dbSNP: rs10757269
rs10757269
CDKN2B-AS1
1.000 0.040 9 22072265 intron variant A/C;G snv
CUI: C1328319
Disease: Ankle brachial pressure index (observable entity)
Ankle brachial pressure index (observable entity) 		0.800 1.000 1 2012 2012