|
CDKN2B-AS1
|
0.150 |
GeneticVariation
|
disease |
BEFREE |
Recent genome-wide association studies have established that polymorphisms within CDKN2B-AS1 of chr9p21.3 locus increased susceptibility to coronary artery disease (CAD) or myocardial infarction.
|
30587704 |
2019 |
|
CDKN2B-AS1
|
0.150 |
GeneticVariation
|
disease |
BEFREE |
Here we investigate whether the variants on ANRIL promoter and exons have an effect on myocardial infarction (MI) risk, and further analyze the association of these variants with the expression of ANRIL transcript.
|
28107200 |
2017 |
|
CDKN2B-AS1
|
0.150 |
GeneticVariation
|
disease |
GWASCAT |
A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.
|
26708285 |
2016 |
|
CDKN2B-AS1
|
0.150 |
GeneticVariation
|
disease |
BEFREE |
Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.
|
26999117 |
2016 |
|
CDKN2B-AS1
|
0.150 |
GeneticVariation
|
disease |
GWASCAT |
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
|
26343387 |
2015 |
|
CDKN2B-AS1
|
0.150 |
GeneticVariation
|
disease |
BEFREE |
Comparisons of allele frequencies by the χ(2) test revealed that rs9369640 of the phosphatase and actin regulator 1 gene (PHACTR1, FDR=0.0007), rs4977574 of the CDKN2B antisense RNA 1 gene (CDKN2B-AS1, FDR=0.0038), rs264 of the lipoprotein lipase gene (LPL, FDR=0.0061), rs599839 of the proline/serine-rich coiled-coil 1 gene (PSRC1, FDR=0.0118), rs9319428 of the fms-related tyrosine kinase 1 gene (FLT1, FDR=0.0118) and rs12413409 of the cyclin and CBS domain divalent metal cation transport mediator 2 gene (CNNM2, FDR=0.0300) were significantly associated with MI.
|
25738804 |
2015 |
|
CDKN2B-AS1
|
0.150 |
Biomarker
|
disease |
BEFREE |
ANRIL (antisense Non-coding RNA in the INK4 Locus (harboring the CDKN2A/B genes)) variants were related to a variety of vascular diseases (myocardial infarction, aortic and intracranial aneurysm), including ischaemic stroke.
|
22776031 |
2012 |
|
CDKN2B-AS1
|
0.150 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
CDKN2B-AS1
|
0.150 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
|
19198609 |
2009 |
|
CDKN2B-AS1
|
0.150 |
GeneticVariation
|
disease |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
CDKN2B-AS1
|
0.150 |
GeneticVariation
|
disease |
GWASCAT |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |