rs1333049, CDKN2B-AS1

N. diseases: 60
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.
Arterial aneurysm
CUI: C0340613
Disease: Arterial aneurysm
2 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2009 2009
Carotid artery calcification
CUI: C4285890
Disease: Carotid artery calcification
3 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2015 2015
Post MI
CUI: C0856742
Disease: Post MI
4 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2009 2009
Arteriosclerotic cardiovascular disease, NOS
CUI: C3665365
Disease: Arteriosclerotic cardiovascular disease, NOS
5 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2017 2017
Peripheral arterial stenosis
CUI: C4025272
Disease: Peripheral arterial stenosis
5 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2017 2017
recurrent myocardial infarction
CUI: C4290140
Disease: recurrent myocardial infarction
6 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2014 2014
Brain Diseases
CUI: C0006111
Disease: Brain Diseases
10 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1 2017 2017
Severe periodontitis
CUI: C4025886
Disease: Severe periodontitis
12 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2020 2020
SPHEROCYTOSIS, TYPE 1 (disorder)
CUI: C2674218
Disease: SPHEROCYTOSIS, TYPE 1 (disorder)
16 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2017 2017
Peripheral Vascular Diseases
CUI: C0085096
Disease: Peripheral Vascular Diseases
18 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2011 2011
Aortic Valve Stenosis
CUI: C0003507
Disease: Aortic Valve Stenosis
19 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2019 2019
Angina, Unstable
CUI: C0002965
Disease: Angina, Unstable
21 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2018 2018
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
32 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2011 2011
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2013 2013
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2011 2011
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2017 2017
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1 2009 2009
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.020 1.000 2 2008 2016
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.020 1.000 2 2010 2014
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.030 1.000 3 2009 2014
Small cell carcinoma of lung
CUI: C0149925
Disease: Small cell carcinoma of lung
125 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2016 2016
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2017 2017
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.040 1.000 4 2010 2014