rs10757278, CDKN2B-AS1

N. diseases: 44
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.
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.900 0.923 13 2007 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.100 0.958 24 2008 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.800 1.000 13 2008 2016
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.040 0.750 4 2008 2014
Intracranial Aneurysm
CUI: C0007766
Disease: Intracranial Aneurysm
150 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.030 0.667 3 2008 2014
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.020 1.000 2 2008 2017
Familial cervical artery dissection
CUI: C4755308
Disease: Familial cervical artery dissection
2 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2008 2008
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.070 1.000 7 2009 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.040 0.750 4 2009 2012
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.030 1.000 3 2009 2016
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.020 1.000 2 2009 2016
Aortic Aneurysm
CUI: C0003486
Disease: Aortic Aneurysm
19 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2009 2009
Aortic aneurysm without mention of rupture NOS
CUI: C0340629
Disease: Aortic aneurysm without mention of rupture NOS
4 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2009 2009
Arterial aneurysm
CUI: C0340613
Disease: Arterial aneurysm
2 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2009 2009
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2009 2009
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2009 2009
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2009 2009
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2009 2009
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.080 0.875 8 2010 2020
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2010 2010
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2010 2010
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.700 1.000 3 2011 2013
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2011 2011
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
269 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2011 2011
Peripheral Vascular Diseases
CUI: C0085096
Disease: Peripheral Vascular Diseases
18 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2011 2011