|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
While we confirmed the association of rs10757278 with CDKN2B expression in MI patients, we failed to find an association between the investigated variants and MI or disease burden.
|
31386834 |
2019 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
The aim of the study was to find whether patients carrying polymorphic allele of the rs10757278 polymorphism from 9p21 locus have changed risk of arrhythmia (atrial fibrillation, AF; sustained ventricular tachycardia or ventricular fibrillation, sVT/VF) during acute phase of myocardial infarction.
|
26615606 |
2016 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
We found even more significant association between rs</span>10757278 polymorphism and MI in pooled population, p = 3.55 × 10-53, after excluding the study from the Pakistan population.
|
26006241 |
2015 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Genome-wide association studies have identified 2 single-nucleotide polymorphisms (SNPs) on chromosome arm 9p21, rs10757278, and rs2383207 that confer susceptibility to myocardial infarction.
|
23454037 |
2013 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
We replicated the association between the rs10757278 SNP and myocardial infarction and binary (presence/absence) angiographic classifications of CAD.
|
20729229 |
2010 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Background Two single nucleotide polymorphisms (SNPs, rs10757278 and rs2383207) on chromosome 9p21 have been proved to be associated with myocardial infarction.
|
18459066 |
2009 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
We related SNPs rs2383207 and rs10757278 to stroke and to myocardial infarction and coronary revascularizations (coronary events) using crude and multivariate adjusted Cox proportional hazards models.
|
19293724 |
2009 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
A common variant at chromosome 9p21 (tagged by the rs1333049 or rs10757278 single-nucleotide polymorphism) is strongly associated with myocardial infarction and major arterial aneurysms.
|
20031606 |
2009 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
This study presents the first analysis of these SNPs (rs10757274, rs2383206, rs2383207, and rs10757278) in a premature, familial CAD/MI population (GeneQuest).
|
18505420 |
2008 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Genome-wide single nucleotide polymorphism (SNP) association studies recently identified four SNPs (rs10757274, rs2383206, rs2383207, and rs10757278) on chromosome 9p21 that were associated with coronary artery disease (CAD) and myocardial infarction (MI) in Caucasian populations from northern Europe and North America.
|
18066490 |
2008 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Recent genome-wide association studies have identified 4 SNPs on chromosome 9p21 associated with CAD (rs10757274 and rs2383206) and myocardial infarction (MI: rs2383207 and rs10757278) in White populations in Northern Europe and North America.
|
18048766 |
2008 |
|
rs10757278
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Recent genome wide association (GWA) studies identified two Single Nucleotide Polymorphisms (SNP) (rs10757278 and rs10757274) in the region of the CDK2NA and CDK2NB genes to be consistently associated with the risks of coronary heart disease (CHD) and myocardial infarction (MI).
|
18925945 |
2008 |
|
rs10757278
|
|
G |
0.900 |
GeneticVariation |
GWASCAT |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |
|
rs10757278
|
|
G |
0.900 |
GeneticVariation |
GWASDB |
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
17478679 |
2007 |