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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.900 0.944 36 2007 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.900 1.000 28 2007 2020
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
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.740 1.000 5 2008 2020
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.740 1.000 5 2008 2020
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.720 1.000 4 2009 2016
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Body mass index
CUI: C1305855
Disease: Body mass index
2689 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2013 2013
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
High density lipoprotein measurement
1440 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2013 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2011 2011
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.700 1.000 1 2016 2016
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.100 1.000 15 2008 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.090 1.000 9 2007 2017
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.040 1.000 4 2010 2014
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.030 1.000 3 2009 2014