|
rs2383206
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Further subgroup analyses showed that rs1333040, rs1333049 and rs2383207 polymorphisms were significantly correlated with the risk of CAD in East Asians, rs2383206 and rs10757274 polymorphisms were significantly correlated with the risk of CAD in West Asians, while rs2383206, rs10757274 and rs10757278 polymorphisms were significantly correlated with the risk of CAD in Caucasians.
|
30814313 |
2019 |
|
rs2383206
|
|
|
0.090 |
GeneticVariation |
BEFREE |
The current study showed that rs10757278/rs2383206-G allele increases the risk for CAD in Egyptians.
|
28559532 |
2017 |
|
rs2383206
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Human aortic smooth muscle cells (HuAoSMCs) were transfected with siRNA targeting ANRIL exon 19 (siRNA-1) or exon 2 (siRNA-2) and consequent effect determined. rs2383206 showed the highest association with CAD (odds ratio [OR] 2.02, 95% confidence interval [CI] 1.56 -2.62) and an adjusted OR of 2.55, 1.33-2.88 along with rs10757278.
|
24452806 |
2014 |
|
rs2383206
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Eight SNPs (rs11206510, rs10118757, rs2383206, rs501120, rs2075292, rs174547, rs173539, and rs255052) were nominally significantly associated with CAD (P<0.05), and 5 of them were newly reported.
|
22664640 |
2012 |
|
rs2383206
|
|
|
0.090 |
GeneticVariation |
BEFREE |
In patients with established CAD, we observed an association between the rs2383206 and higher incidence of overall mortality and death from cardiac causes in patients with multi-vessel CAD.
|
22856518 |
2012 |
|
rs2383206
|
|
|
0.090 |
GeneticVariation |
BEFREE |
We investigated whether the coronary artery disease (CAD) locus on chromosome 9p21 (as represented by single nucleotide polymorphism rs2383206) is associated with low estimated glomerular filtration rate (eGFR) or increased urinary albumin excretion in patients with Type 2 diabetes mellitus (T2DM).
|
22622453 |
2012 |
|
rs2383206
|
|
|
0.090 |
GeneticVariation |
BEFREE |
We found that three of these SNPs (rs10116277, rs1333040 and rs2383206) present at the locus 9p21 were significantly associated with CAD even after controlling for the confounding factors such as age, sex, body mass index, homocysteine, hypertension, diabetes, smoking, diet, etc.
|
20718794 |
2011 |
|
rs2383206
|
|
|
0.090 |
GeneticVariation |
BEFREE |
In contrast, rs2383206</span> was associated with CAD/no MI compared with non-CAD (set 2A: P trend=0.0001; set 2B: P trend=0.0008).
|
19956784 |
2008 |
|
rs2383206
|
|
|
0.090 |
GeneticVariation |
BEFREE |
For the case-control study, association between single-nucleotide polymorphism rs2383206 and CAD defined as angiographically documented stenosis greater than 50% in a major coronary artery or a main branch thereof was assessed and for the cohort study, cumulative 10-year mortality was documented.
|
19033589 |
2008 |