|
rs599839
|
|
|
0.850 |
GeneticVariation |
BEFREE |
The frequency of the protective G-allele of the rs599839 polymorphism was lower in HeFH patients with CHD compared with those HeFH patients without CHD.
|
29714125 |
2018 |
|
rs599839
|
|
|
0.850 |
GeneticVariation |
BEFREE |
No significant associations were observed between the other two SNPs in loci 1p13 (rs599839 and rs646776) and CHD mortality in either gender.
|
24728607 |
2014 |
|
rs599839
|
|
|
0.850 |
GeneticVariation |
GWASCAT |
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
|
24262325 |
2014 |
|
rs599839
|
|
|
0.850 |
GeneticVariation |
BEFREE |
Since genome-wide association studies demonstrated association between rs599839 polymorphism and coronary artery disease, in the present study we assessed the potential association of this polymorphism with endothelial dysfunction, an early step in atherogenesis.
|
22380622 |
2012 |
|
rs599839
|
|
|
0.850 |
GeneticVariation |
BEFREE |
SORT1 rs599839 was associated with CHD risk (OR 1.20; 1.15-1.26) as well as total- and LDL-cholesterol, and apolipoprotein B. ANGPTL3 rs12042319 was associated with CHD risk (OR 1.11; 1.03, 1.19), total- and LDL-cholesterol, triglycerides, and interleukin-6.
|
21804106 |
2012 |
|
rs599839
|
|
|
0.850 |
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 |
|
rs599839
|
|
A |
0.850 |
GeneticVariation |
GWASCAT |
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
|
21378990 |
2011 |
|
rs599839
|
|
A |
0.850 |
GeneticVariation |
GWASDB |
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
|
21378990 |
2011 |
|
rs599839
|
|
|
0.850 |
GeneticVariation |
BEFREE |
In the LURIC Study the G-allele of rs599839 is associated with LDL and TRIG metabolism and the risk of coronary artery disease and myocardial infarction.
|
19837406 |
2010 |
|
rs599839
|
|
A |
0.850 |
GeneticVariation |
GWASDB |
The combined analysis of the two studies identified four additional loci significantly associated with coronary artery disease (P<1.3x10(-6)) and a high probability (>80%) of a true association: chromosomes 1p13.3 (rs599839), 1q41 (rs17465637), 10q11.21 (rs501120), and 15q22.33 (rs17228212).
|
17634449 |
2007 |
|
rs599839
|
|
A |
0.850 |
GeneticVariation |
GWASCAT |
The combined analysis of the two studies identified four additional loci significantly associated with coronary artery disease (P<1.3x10(-6)) and a high probability (>80%) of a true association: chromosomes 1p13.3 (rs599839), 1q41 (rs17465637), 10q11.21 (rs501120), and 15q22.33 (rs17228212).
|
17634449 |
2007 |