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.
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
recurrent myocardial infarction
CUI: C4290140
Disease: recurrent myocardial infarction
6 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2014 2014
Severe periodontitis
CUI: C4025886
Disease: Severe periodontitis
12 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2020 2020
Small cell carcinoma of lung
CUI: C0149925
Disease: Small cell carcinoma of lung
125 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2016 2016
SPHEROCYTOSIS, TYPE 1 (disorder)
CUI: C2674218
Disease: SPHEROCYTOSIS, TYPE 1 (disorder)
16 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2017 2017
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2019 2019
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2011 2011