rs2383207, CDKN2B-AS1

N. diseases: 22
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.
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.800 1.000 1 2010 2010
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.770 1.000 8 2007 2013
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.700 1.000 2 2011 2013
Ankle brachial pressure index (observable entity)
CUI: C1328319
Disease: Ankle brachial pressure index (observable entity)
40 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.700 1.000 1 2012 2012
Glaucoma, Open-Angle
CUI: C0017612
Disease: Glaucoma, Open-Angle
236 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.700 1.000 1 2012 2012
Glioma
CUI: C0017638
Disease: Glioma
353 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.700 1.000 1 2011 2011
Intracranial Aneurysm
CUI: C0007766
Disease: Intracranial Aneurysm
150 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.700 1.000 1 2010 2010
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.100 1.000 10 2008 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.040 1.000 4 2008 2018
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.040 0.750 4 2013 2020
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.030 1.000 3 2009 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.030 1.000 3 2009 2018
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.020 1.000 2 2012 2015
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.020 1.000 2 2012 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.020 1.000 2 2009 2016
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.010 1.000 1 2011 2011
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.010 1.000 1 2009 2009
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.010 1.000 1 2015 2015
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.010 1.000 1 2009 2009
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.010 1.000 1 2013 2013
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.010 1.000 1 2013 2013
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.010 1.000 1 2009 2009