rs1333040, CDKN2B-AS1

N. diseases: 15
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.
Intracranial Aneurysm
CUI: C0007766
Disease: Intracranial Aneurysm
150 0.732 0.280 9 22083405 intron variant C/G;T snv 0.840 1.000 6 2008 2015
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.732 0.280 9 22083405 intron variant C/G;T snv 0.720 0.667 3 2007 2011
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.732 0.280 9 22083405 intron variant C/G;T snv 0.700 1.000 1 2011 2011
Glaucoma, Open-Angle
CUI: C0017612
Disease: Glaucoma, Open-Angle
236 0.732 0.280 9 22083405 intron variant C/G;T snv 0.700 1.000 1 2012 2012
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.732 0.280 9 22083405 intron variant C/G;T snv 0.700 1.000 1 2017 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.732 0.280 9 22083405 intron variant C/G;T snv 0.050 1.000 5 2011 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.732 0.280 9 22083405 intron variant C/G;T snv 0.030 1.000 3 2011 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.732 0.280 9 22083405 intron variant C/G;T snv 0.020 0.500 2 2012 2013
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.732 0.280 9 22083405 intron variant C/G;T snv 0.020 1.000 2 2011 2014
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.732 0.280 9 22083405 intron variant C/G;T snv 0.020 1.000 2 2013 2016
Seizures
CUI: C0036572
Disease: Seizures
553 0.732 0.280 9 22083405 intron variant C/G;T snv 0.020 1.000 2 2013 2014
Arteriovenous hemangioma
CUI: C0334533
Disease: Arteriovenous hemangioma
14 0.732 0.280 9 22083405 intron variant C/G;T snv 0.010 1.000 1 2013 2013
Congenital arteriovenous malformation
CUI: C0003857
Disease: Congenital arteriovenous malformation
23 0.732 0.280 9 22083405 intron variant C/G;T snv 0.010 1.000 1 2013 2013
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.732 0.280 9 22083405 intron variant C/G;T snv 0.010 1.000 1 2010 2010
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.732 0.280 9 22083405 intron variant C/G;T snv 0.010 1.000 1 2012 2012