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.
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
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
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
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
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
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
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
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
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
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
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
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.900 0.923 13 2007 2019
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
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.020 1.000 2 2012 2017
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.700 1.000 1 2013 2013
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.080 0.875 8 2010 2020
Intracranial Aneurysm
CUI: C0007766
Disease: Intracranial Aneurysm
150 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.030 0.667 3 2008 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.030 1.000 3 2009 2016
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
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
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.020 1.000 2 2008 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.800 1.000 13 2008 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.100 0.958 24 2008 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.070 1.000 7 2009 2016