rs10757274, 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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.900 1.000 11 2008 2016
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.700 1.000 2 2013 2013
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.700 1.000 1 2017 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.100 1.000 11 2009 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.090 1.000 9 2008 2018
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.030 1.000 3 2009 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.030 0.667 3 2016 2018
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.030 1.000 3 2009 2019
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.020 0.500 2 2012 2012
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.020 1.000 2 2009 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.020 1.000 2 2013 2015
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.020 1.000 2 2009 2013
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2012 2012
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2012 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2012 2012
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2009 2009
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2009 2009
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2009 2009
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2012 2012
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2012 2012
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2009 2009
recurrent myocardial infarction
CUI: C4290140
Disease: recurrent myocardial infarction
6 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2012 2012