rs4977756, CDKN2B-AS1

N. diseases: 24
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.
Glioma
CUI: C0017638
Disease: Glioma
353 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.900 0.875 16 2009 2020
Glaucoma, Open-Angle
CUI: C0017612
Disease: Glaucoma, Open-Angle
236 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.810 1.000 3 2011 2014
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.800 1.000 1 2011 2011
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.710 1.000 2 2010 2016
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.700 1.000 2 2011 2013
Central Nervous System Neoplasms
CUI: C0085136
Disease: Central Nervous System Neoplasms
72 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.700 1.000 2 2009 2012
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
36 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.020 1.000 2 2016 2020
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2014 2014
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2016 2016
Adult Medulloblastoma
CUI: C0278876
Disease: Adult Medulloblastoma
24 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2018 2018
Asthma
CUI: C0004096
Disease: Asthma
1536 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2010 2010
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1 2013 2013
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2014 2014
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2016 2016
Childhood Medulloblastoma
CUI: C0278510
Disease: Childhood Medulloblastoma
25 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2018 2018
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2016 2016
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2014 2014
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
115 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2018 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2018 2018
Piebaldism
CUI: C0080024
Disease: Piebaldism
18 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2015 2015
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2014 2014
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.010 1.000 1 2014 2014