Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.900 0.923 12 2007 2019
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 10 2008 2016
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.100 0.958 24 2008 2019
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.080 0.875 8 2010 2020
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.070 1.000 7 2009 2016
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal 		0.040 0.750 4 2008 2014
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.040 0.750 4 2009 2012
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		0.040 1.000 4 2012 2014
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.030 0.667 3 2008 2014
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 1.000 3 2009 2016
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.020 1.000 2 2009 2016
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.020 1.000 2 2012 2017
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 1.000 2 2008 2017
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2012 2017
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		0.020 1.000 2 2013 2014
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.010 1.000 1 2011 2011
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		0.010 1.000 1 2016 2016
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2010 2010
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.010 1.000 1 2020 2020
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.010 1.000 1 2009 2009
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
Premature coronary artery atherosclerosis 		0.010 1.000 1 2012 2012
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation 		0.010 1.000 1 2016 2016
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2010 2010
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs10757278
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C4290140
Disease: recurrent myocardial infarction
recurrent myocardial infarction 		0.010 1.000 1 2012 2012