rs9349379
|
|
|
0.760 |
GeneticVariation |
BEFREE |
Our meta-analysis suggested that rs9349379 polymorphism might affect individual susceptibility to CAD in both Caucasians and Asians.
|
31278837 |
2019 |
rs9349379
|
|
|
0.760 |
GeneticVariation |
BEFREE |
Our study indicate that the PHACTR1 rs9349379 polymorphism is associated with the increased risk for CAD in the female Chinese Han population.
|
30777881 |
2019 |
rs9349379
|
|
G |
0.760 |
GeneticVariation |
GWASCAT |
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
|
30104761 |
2018 |
rs9349379
|
|
|
0.760 |
GeneticVariation |
BEFREE |
This result suggests that rs9349379 may in part influence CAD by modulating the expression of intermediate PHACTR1 transcripts in endothelial or vascular smooth muscle cells found in hCA.
|
29884117 |
2018 |
rs9349379
|
|
A |
0.760 |
GeneticVariation |
GWASCAT |
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
|
29212778 |
2018 |
rs9349379
|
|
G |
0.760 |
GeneticVariation |
GWASCAT |
Association analyses based on false discovery rate implicate new loci for coronary artery disease.
|
28714975 |
2017 |
rs9349379
|
|
G |
0.760 |
GeneticVariation |
GWASCAT |
Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease.
|
28714974 |
2017 |
rs9349379
|
|
|
0.760 |
GeneticVariation |
BEFREE |
The top variant, rs9349379, is intronic to PHACTR1, a risk locus for coronary artery disease, migraine, and cervical artery dissection.
|
27792790 |
2016 |
rs9349379
|
|
|
0.760 |
GeneticVariation |
BEFREE |
In summary, our results suggest that the PHACTR1 rs9349379 polymorphism plays an important role in the risk of developing premature CAD in the Mexican population.
|
27517945 |
2016 |
rs9349379
|
|
|
0.760 |
GeneticVariation |
BEFREE |
In primary human macrophages, we identified a novel expression quantitative trait locus (eQTL) specific for this short transcript, whereby the risk allele at CAD risk SNP rs9349379 is associated with reduced PHACTR1 expression, similar to the effect of an inflammatory stimulus.
|
27187934 |
2016 |
rs9349379
|
|
G |
0.760 |
GeneticVariation |
GWASCAT |
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
|
26343387 |
2015 |