|
rs2459976
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We conclude that rs2459976 in the <i>ZW10</i> gene is associated with CHD in Chinese Han populations.
|
29423089 |
2018 |
|
rs6918631
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of coronary artery disease in the Japanese.
|
21971053 |
2012 |
|
rs9295769
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of coronary artery disease in the Japanese.
|
21971053 |
2012 |
|
rs2075291
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The single nucleotide polymorphism, 553G>T, was found to correlate with the severity of CHD in males (P=0.032).
|
23970179 |
2013 |
|
rs964184
|
|
|
0.830 |
GeneticVariation |
BEFREE |
MG 18∶2 showed an enrichment (P-value = 0.002) of significant associations with CHD-associated SNPs (P-value = 1.2×10-7 for association with rs964184 in the ZNF259/APOA5 region) and a weak, but positive causal effect (odds ratio = 1.05 per SD increment in MG 18∶2, P-value = 0.05) on CHD, as suggested by Mendelian randomization analysis.
|
25502724 |
2014 |
|
rs964184
|
|
G |
0.830 |
GeneticVariation |
GWASDB |
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
|
21378990 |
2011 |
|
rs964184
|
|
|
0.830 |
GeneticVariation |
GWASCAT |
Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases.
|
27790247 |
2016 |
|
rs964184
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Our results indicate that both gender and age have great impacts on the association of the rs964184 polymorphism with CHD among Chinese.
|
29339699 |
2018 |
|
rs964184
|
|
|
0.830 |
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 |
|
rs964184
|
|
|
0.830 |
GeneticVariation |
GWASCAT |
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
|
24262325 |
2014 |
|
rs964184
|
|
G |
0.830 |
GeneticVariation |
GWASCAT |
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
|
21378990 |
2011 |
|
rs964184
|
|
|
0.830 |
GeneticVariation |
BEFREE |
Recently, the rs964184 polymorphism has been associated with coronary artery disease in nonrheumatic Caucasian individuals.
|
24131021 |
2013 |
|
rs6589566
|
|
|
0.700 |
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 |
|
rs3757333
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of coronary artery disease in the Japanese.
|
21971053 |
2012 |
|
rs16982520
|
|
|
0.700 |
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 |
|
rs16948048
|
|
|
0.700 |
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 |
|
rs4804611
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Nine loci were statistically associated with incident CHD events in white participants: 9p21 (rs10757278; P=4.7 × 10(-41)), 16q23.1 (rs2549513; P=0.0004), 6p24.1 (rs499818; P=0.0002), 2q36.3 (rs2943634; P=6.7 × 10(-6)), MTHFD1L (rs6922269, P=5.1 × 10(-10)), APOE (rs429358; P=2.7×10(-18)), ZNF627 (rs4804611; P=5.0 × 10(-8)), CXCL12 (rs501120; P=1.4 × 10(-6)) and LPL (rs268; P=2.7 × 10(-17)).
|
22042884 |
2011 |
|
rs16998248
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The polymorphisms rs16998248 (T>A) and rs35720349 (C>T) in coronary artery disease have been associated with reduced expression of ZNF217.
|
25729968 |
2015 |
|
rs35720349
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The polymorphisms rs16998248 (T>A) and rs35720349 (C>T) in coronary artery disease have been associated with reduced expression of ZNF217.
|
25729968 |
2015 |
|
rs9468076
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of coronary artery disease in the Japanese.
|
21971053 |
2012 |
|
rs10484404
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study of coronary artery disease in the Japanese.
|
21971053 |
2012 |
|
rs121908603
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The other two mutations (p.M703L and p.Q889E) were reported in patients with congenital diaphragmatic hernia but not in patients with CHD.
|
21919901 |
2012 |
|
rs146423225
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The other two mutations (p.M703L and p.Q889E) were reported in patients with congenital diaphragmatic hernia but not in patients with CHD.
|
21919901 |
2012 |
|
rs7190256
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases.
|
27790247 |
2016 |
|
rs16971436
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Stratification analysis indicated that the risks of AF were statistically different among subgroups of age for rs2106261, and the effect for rs16971436 was more evident in subgroups of patients with coronary artery disease.
|
24983873 |
2014 |