Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11206510
rs11206510 		0.810 GeneticVariation BEFREE Two-sided <i>P</i> values <0.05 were considered significant.<b>Results:</b> We observed a significant interaction between the <i>PCSK9</i> rs11206510 genotype and LC n-3 PUFA intake on nonfatal MI risk (<i>P</i>-interaction = 0.012). 28330911

2017
dbSNP: rs11206510
rs11206510 		T 0.810 GeneticVariation GWASCAT A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. 26343387

2015
dbSNP: rs11206510
rs11206510 		T 0.810 GeneticVariation GWASCAT Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609

2009
dbSNP: rs11206510
rs11206510 		T 0.810 GeneticVariation GWASDB Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609

2009