Variant: rs471364 

    present in Gene: TTC39B
    present in Chromosome: 9
    Position on Chromosome: 15289580
    Alleles of this Variant: C/T

rs471364 in TTC39B gene and Coronary heart disease PMID 21347282 2011 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

rs471364 in TTC39B gene and High density lipoprotein measurement PMID 19060906 2009 Common variants at 30 loci contribute to polygenic dyslipidemia.

rs471364 in TTC39B gene and Serum HDL cholesterol measurement PMID 19060906 2009 Common variants at 30 loci contribute to polygenic dyslipidemia.