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.
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
Brain Diseases
CUI: C0006111
Disease: Brain Diseases
10 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1 2017 2017
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
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: 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
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
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
CUI: C0392885
Disease: 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
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
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 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
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
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