Variant: rs1122608 

    present in Gene: SMARCA4
    present in Chromosome: 19
    Position on Chromosome: 11052925
    Alleles of this Variant: G/T

rs1122608 in SMARCA4 gene and CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 PMID 23202125 2013 Large-scale association analysis identifies new risk loci for coronary artery disease.

rs1122608 in SMARCA4 gene and Cerebrovascular accident PMID 24262325 2014 Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.

rs1122608 in SMARCA4 gene and Coronary Artery Disease PMID 24262325 2014 Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.

rs1122608 in SMARCA4 gene and Coronary heart disease PMID 21378990 2011 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

PMID 24262325 2014 Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.

PMID 21347282 2011 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

rs1122608 in SMARCA4 gene and Low density lipoprotein cholesterol measurement PMID 23202125 2013 Large-scale association analysis identifies new risk loci for coronary artery disease.

rs1122608 in SMARCA4 gene and Myocardial Infarction PMID 19198609 2009 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.

rs1122608 in SMARCA4 gene and Serum LDL cholesterol measurement PMID 23202125 2013 Large-scale association analysis identifies new risk loci for coronary artery disease.

rs1122608 in SMARCA4 gene and Serum total cholesterol measurement PMID 23202125 2013 Large-scale association analysis identifies new risk loci for coronary artery disease.