|
rs1000778
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The rs1000778 minor allele AA was associated with a lower risk of CAD (OR =0.37, 95% CI: 0.15-0.89, P=0.025).
|
28237083 |
2017 |
|
rs10033464
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Two hundred and sixty-seven individuals comprising of 170 patients with Coronary Artery Disease (CAD), 41 patients with AF, and 56 healthy controls were genotyped for rs10033464 and rs2200733 at 4q25 locus.
|
27346453 |
2017 |
|
rs10033601
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The results of this study indicate that variations in the lipid regulatory pathway genes FBXW7 and SREBPs (rs9902941 in SREBP-1, rs7288536 in SREBP-2 and rs10033601 in FBXW7) are associated with CAD in the Uygur Chinese population in Xinjiang, China.
|
29152152 |
2017 |
|
rs1004467
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The CC genotype of rs1004467 and the AA genotype of rs4919687 could be risk genetic markers of CAD in women.
|
25889125 |
2015 |
|
rs1004467
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Polymorphisms rs4919686, rs4919687 and rs1004467 were found to be associated with CAD in this Uygur population.
|
25592814 |
2015 |
|
rs1004638
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the first study, rs2383206, rs1004638, and rs10757278 in block 3 were significantly associated with CAD but not with ischemic stroke independent of traditional cardiovascular risk factors in additive model (P = 0.002 to 0.0001, q = 0.026 to 0.004).
|
20031605 |
2009 |
|
rs1007888
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The polymorphism of MIF gene (rs755622 [-173G/C], rs1007888, and rs2096525) were genotyped by TaqMan single nucleotide polymorphism (SNP) genotyping assay in 320 patients with coronary artery disease (CAD) and 603 controls in a Chinese Kazakh population.
|
26825917 |
2016 |
|
rs1008949
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The distribution of rs1008949 genotypes, dominant model, recessive model, and allele frequency did not show a significant difference between patients with CAD and the control subjects in the Han and Uygur groups.
|
24886494 |
2014 |
|
rs10093110
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
|
rs1010
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We considered five variants that were associated with coronary heart disease in two studies and confirmed in the Atherosclerosis Risk in Communities study: rs20455 (KIF6), rs3900940 (MYH15), rs7439293 (PALLD), rs2298566 (SNX19), and rs1010 (VAMP8).
|
18073581 |
2007 |
|
rs10106652
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
|
rs10116253
|
|
|
0.010 |
GeneticVariation |
BEFREE |
RESULTS TLR4 rs10116253 in the promoter region was associated with CAD risk</span>.
|
28092654 |
2017 |
|
rs10116277
|
|
|
0.010 |
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 |
|
rs10118757
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Our study firstly reported that SNP rs10118757 was associated with CAD risk in a Chinese Han population, indicating that MTAP gene may play a potential role in the pathophysiological process of CAD.
|
23462334 |
2013 |
|
rs10118757
|
|
|
0.020 |
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 |
|
rs10128951
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
|
rs10131519
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
|
rs10131894
|
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
|
rs10139550
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Association analyses based on false discovery rate implicate new loci for coronary artery disease.
|
28714975 |
2017 |
|
rs10139550
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
|
26343387 |
2015 |
|
rs10159239
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The Single Nucleotide Polymorphism rs10159239 was examined by logistic regression with known risk factors for Coronary artery disease and remained significant (0.035).
|
31639433 |
2020 |
|
rs1018383
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A haplotype AGCG (constructed by rs2076188, rs7753407, rs11966356 and rs1018383) was identified to protect subjects from early-onset CAD (OR = 0.332, 95% CI = 0.105-0.879, adjusted P = 0.010).
|
26375920 |
2015 |
|
rs10186133
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
|
rs1020608562
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We investigated the effect of 5 common variations of chemokine and chemokine receptor genes (SDF1-3'A, CCR5-delta32, CCR2-64I, CX3CR1-V249I and CX3CR1-T280M) on predisposition to CAD.
|
16480760 |
2007 |
|
rs10221742
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |