Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9349379
rs9349379
PHACTR1
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
dbSNP: rs9349379
rs9349379
PHACTR1
0.760 GeneticVariation BEFREE Our meta-analysis suggested that rs9349379 polymorphism might affect individual susceptibility to CAD in both Caucasians and Asians. 31278837

2019
dbSNP: rs9349379
rs9349379
PHACTR1
G 0.760 GeneticVariation GWASCAT Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. 30104761

2018
dbSNP: rs9349379
rs9349379
PHACTR1
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
dbSNP: rs9349379
rs9349379
PHACTR1
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
dbSNP: rs9349379
rs9349379
PHACTR1
G 0.760 GeneticVariation GWASCAT Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease. 28714974

2017
dbSNP: rs9349379
rs9349379
PHACTR1
G 0.760 GeneticVariation GWASCAT Association analyses based on false discovery rate implicate new loci for coronary artery disease. 28714975

2017
dbSNP: rs9349379
rs9349379
PHACTR1
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
dbSNP: rs9349379
rs9349379
PHACTR1
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
dbSNP: rs9349379
rs9349379
PHACTR1
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
dbSNP: rs9349379
rs9349379
PHACTR1
G 0.760 GeneticVariation GWASCAT A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. 26343387

2015