|
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 |
A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.
|
21606135 |
2011 |
|
rs1333049
|
|
C |
0.900 |
GeneticVariation |
GWASDB |
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 of a coronary artery disease risk variant.
|
23364394 |
2013 |
|
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 |
Association Study Between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian Population.
|
28639227 |
2017 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Despite excellent power, the 9p21 locus SNP (rs1333049) was only modestly associated with MI (HR = 1.09, p-value = 0.02) and marginally with CHD (HR = 1.06, p-value = 0.08).
|
26950853 |
2016 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Gender-based subgroup tests showed that four polymorphisms (rs75227345, rs2383205, rs10738606 and rs1333049) were associated with CHD in males (p < .05).
|
31496134 |
2019 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
GWASDB |
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
|
22751097 |
2012 |
|
rs1333049
|
|
C |
0.900 |
GeneticVariation |
GWASDB |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
rs1333049
|
|
C |
0.900 |
GeneticVariation |
GWASCAT |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
|
17554300 |
2007 |
|
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
|
|
|
0.900 |
GeneticVariation |
BEFREE |
However, the effect of rs1333049 on clinical outcomes in patients with established coronary disease has yet to be determined.
|
20400779 |
2010 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Independent association of the variant rs1333049 at the 9p21 locus and coronary heart disease.
|
21874923 |
2011 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
GWASDB |
Large-scale gene-centric analysis identifies novel variants for coronary artery disease.
|
21966275 |
2011 |
|
rs1333049
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Of thousands of chromosomal loci studied, the same locus had the strongest association with coronary artery disease in both the WTCCC and the German studies: chromosome 9p21.3 (SNP, rs1333049) (P=1.80x10(-14) and P=3.40x10(-6), respectively).
|
17634449 |
2007 |
|
rs1333049
|
|
C |
0.900 |
GeneticVariation |
GWASDB |
Of thousands of chromosomal loci studied, the same locus had the strongest association with coronary artery disease in both the WTCCC and the German studies: chromosome 9p21.3 (SNP, rs1333049) (P=1.80x10(-14) and P=3.40x10(-6), respectively).
|
17634449 |
2007 |
|
rs1333049
|
|
C |
0.900 |
GeneticVariation |
GWASCAT |
Of thousands of chromosomal loci studied, the same locus had the strongest association with coronary artery disease in both the WTCCC and the German studies: chromosome 9p21.3 (SNP, rs1333049) (P=1.80x10(-14) and P=3.40x10(-6), respectively).
|
17634449 |
2007 |
|
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 |
Our study aims to explore the association of rs7025486 single-nucleotide polymorphisms (SNP) in DAB2IP and rs1333049 on chromosome 9p21.3 with the coronary artery disease in Chinese population.
|
28962556 |
2017 |
|
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
|
|
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 |
SNP rs1333049 on chromosome 9p21.3 was associated with both CHD and stroke (HR=1.20, 95% CI 1.08-1.34 for incident CHD events and 1.15, 0.99-1.34 for incident stroke).
|
18979498 |
2009 |
|
rs1333049
|
|
|
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 |