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.
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
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
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
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
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
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
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2013 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2018 2018
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
Peripheral Arterial Diseases
CUI: C1704436
Disease: Peripheral Arterial Diseases
128 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2013 2013
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
Polypoidal choroidal vasculopathy
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
67 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2011 2011
Premature coronary artery atherosclerosis
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
43 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2012 2012
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2020 2020
recurrent myocardial infarction
CUI: C4290140
Disease: recurrent myocardial infarction
6 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2012 2012
ST segment elevation myocardial infarction
CUI: C1536220
Disease: ST segment elevation myocardial infarction
16 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
Sustained ventricular tachycardia
CUI: C0750197
Disease: Sustained ventricular tachycardia
1 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
Ventricular Fibrillation
CUI: C0042510
Disease: Ventricular Fibrillation
19 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016