rs1412829, CDKN2B-AS1

N. diseases: 14
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 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.810 1.000 4 2009 2016
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.720 1.000 3 2010 2017
Nasopharyngeal Neoplasms
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
36 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.700 1.000 2 2010 2016
Adult Anaplastic Astrocytoma
CUI: C0280483
Disease: Adult Anaplastic Astrocytoma
8 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.010 1.000 1 2010 2010
Anaplastic astrocytoma
CUI: C0334579
Disease: Anaplastic astrocytoma
12 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.010 1.000 1 2010 2010
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.700 1.000 1 2011 2011
Central Nervous System Neoplasms
CUI: C0085136
Disease: Central Nervous System Neoplasms
72 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.800 1.000 1 2009 2009
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.010 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.010 1.000 1 2008 2008
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.700 1.000 1 2011 2011
Glaucoma, Open-Angle
CUI: C0017612
Disease: Glaucoma, Open-Angle
236 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.700 1.000 1 2012 2012
Grade III Childhood Astrocytoma
CUI: C4551548
Disease: Grade III Childhood Astrocytoma
8 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.010 1.000 1 2010 2010
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.010 1.000 1 2018 2018
Piebaldism
CUI: C0080024
Disease: Piebaldism
18 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.010 1.000 1 2015 2015