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.
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
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
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
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
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
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
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
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
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
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2019 2019
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
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.800 1.000 2 2011 2013
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