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.
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.020 1.000 2 2013 2014
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
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.020 1.000 2 2008 2019
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
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.020 1.000 2 2011 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.020 1.000 2 2008 2016
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2016 2016
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2011 2011
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2010 2010
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
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
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
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2014 2014
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
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 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
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2017 2017
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2020 2020
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
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
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
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2018 2018
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2020 2020
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2013 2013