Variant: rs3846663 

    present in Gene: HMGCR;CERT1
    present in Chromosome: 5
    Position on Chromosome: 75359901
    Alleles of this Variant: C/T

rs3846663 in HMGCR;CERT1 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.

rs3846663 in HMGCR;CERT1 gene and Low density lipoprotein cholesterol measurement PMID 19060906 2009 Common variants at 30 loci contribute to polygenic dyslipidemia.

PMID 31217584 2019 Genetic analyses of diverse populations improves discovery for complex traits.

PMID 19197348 2009 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.

rs3846663 in HMGCR;CERT1 gene and Serum LDL cholesterol measurement PMID 19060906 2009 Common variants at 30 loci contribute to polygenic dyslipidemia.

rs3846663 in HMGCR;CERT1 gene and Serum total cholesterol measurement PMID 31217584 2019 Genetic analyses of diverse populations improves discovery for complex traits.

rs3846663 in HMGCR;CERT1 gene and Triglycerides measurement PMID 19197348 2009 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.