|
rs10757274
|
|
|
0.900 |
GeneticVariation |
BEFREE |
The Ch9p21 SNPs rs1333049 (OR 1.17; 95% confidence limits 1.11-1.24) and rs10757274 (OR 1.17; 1.09-1.26), MIA3 rs17465637 (OR 1.10; 1.04-1.15), Ch2q36 rs2943634 (OR 1.08; 1.03-1.14), APC rs383830 (OR 1.10; 1.02, 1.18), MTHFD1L rs6922269 (OR 1.10; 1.03, 1.16), CXCL12 rs501120 (OR 1.12; 1.04, 1.20), and SMAD3 rs17228212 (OR 1.11; 1.05, 1.17) were all associated with CHD risk, but not with the CHD biomarkers and risk factors measured.
|
21804106 |
2012 |
|
rs10757274
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Although overall, rs10757274 did not add substantially to the usefulness of the FRS for predicting future events, it did improve reclassification of CHD risk, and thus may have clinical utility.
|
18250146 |
2008 |
|
rs10757274
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Interestingly, the haplotype AA (rs10757274 and rs1333042) of CDKN2BAS was associated with decreased the risk of CHD in men (OR = 0.72, 95% CI: 0.55 - 0.95, P = 0.022).
|
27741513 |
2016 |
|
rs10757274
|
|
|
0.900 |
GeneticVariation |
BEFREE |
A case-control study to investigate the association of the 9p21 single nucleotide polymorphisms (SNPs) rs10757274 and rs10757278 (known to be associated with coronary artery disease [CAD] risk) with peripheral arterial disease (PAD), in a Han Chinese population.
|
23569135 |
2013 |
|
rs10757274
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Using the combined TDT/S-TDT test, the 3 single nucleotide polymorphisms (SNP), rs10757274, rs2383206 and rs1333049, were strongly associated with early-onset CHD (p = 2.7 x 10(-6), 2.7 x 10(-6), 3.8 x 10(-7), respectively).
|
18957718 |
2008 |
|
rs10757274
|
|
|
0.900 |
GeneticVariation |
BEFREE |
We confirmed the associations between four polymorphisms and CHD, the rs1151640 polymorphism in the olfactory receptor family 13 subfamily G member 1 (OR13G1) gene (HR 1.14, 95% CI 1.01-1.28, P = 0.03), the rs11881940 polymorphism in the heterogeneous nuclear ribonucleoprotein U-like 1 (HNRPUL1) gene (HR 1.27, 95% CI 1.07-1.51, P = 0.007), the rs3746731 polymorphism in the complement component 1 q subcomponent receptor 1 (CD93) gene (HR 1.26, 95% CI 1.06-1.49, P = 0.01), and the rs10757274 polymorphism near the cyclin-dependent kinase N2A and N2B (CDKN2A and CDKN2B) genes (HR 1.39, 95% CI 1.15-1.69, P < 0.001).
|
18599554 |
2008 |
|
rs10757274
|
|
|
0.900 |
GeneticVariation |
BEFREE |
In an additive model, the age and sex adjusted hazard ratios (HRs) (95% confidence interval) for CHD and MI were 1.03 (0.90, 1.18) and 0.94 (0.82, 1.08) per copy of the G allele of rs10757274.
|
18925945 |
2008 |
|
rs10757274
|
|
G |
0.900 |
GeneticVariation |
GWASDB |
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
|
22751097 |
2012 |
|
rs10757274
|
|
G |
0.900 |
GeneticVariation |
GWASCAT |
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
|
22751097 |
2012 |
|
rs10757274
|
|
|
0.900 |
GeneticVariation |
BEFREE |
A single-nucleotide polymorphism on chromosome 9p21, rs10757274 (9p21 allele), has been shown to predict coronary heart disease (CHD) in whites.
|
20031596 |
2009 |
|
rs10757274
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Association of the rs10757274 SNP with coronary artery disease in a small group of a Pakistani population.
|
25592106 |
2015 |
|
rs10757274
|
|
|
0.900 |
GeneticVariation |
BEFREE |
The GG genotype of rs10757274 on chromosome 9p21, which has been shown to increase CHD risk, is also associated with increased HF risk among whites.
|
19329499 |
2009 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
This study confirms the association between 9p21 (rs1333049) and fatal CHD in a Norwegian population-based cohort.
|
24728607 |
2014 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Our case-control study and meta-analysis suggest that rs1333049 is a useful risk marker of CHD.
|
24930384 |
2014 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Association Study Between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian Population.
|
28639227 |
2017 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
ANRIL polymorphisms (rs1333049 and rs3217992) in relation to plasma CRP levels among in-patients with CHD.
|
31770616 |
2020 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
The leading coronary artery disease-associated SNP rs1333049 was associated with coronary artery disease; however, none of the 9p21 SNP evaluated in the present study were associated with extreme longevity.
|
25257646 |
2015 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
GWASDB |
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.
|
21347282 |
2011 |
|
rs1333049
|
|
C |
0.900 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.
|
21606135 |
2011 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
GWASDB |
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.
|
22319020 |
2012 |
|
rs1333049
|
|
C |
0.900 |
GeneticVariation |
GWASCAT |
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
|
24262325 |
2014 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
We genotyped the rs1333049 single-nucleotide polymorphism in 593 Caucasian individuals with stable coronary artery disease recruited in the Heart and Soul Study.
|
19171343 |
2009 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
GWASCAT |
Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases.
|
27790247 |
2016 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Recent genetic studies identified the rs1333049 variant on chromosome 9p21 as a major susceptibility locus for coronary artery disease and myocardial infarction (MI).
|
20231156 |
2010 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
GWASDB |
A genome-wide association study of a coronary artery disease risk variant.
|
23364394 |
2013 |