rs7703051

This is a intron variant variant.

GWAS Catalog Trait Associations (4)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

low density lipoprotein cholesterol measurement

Allele C
OR 1.90
p 9.0e-33
N 125,692
Large GWAS
multi-ancestry
Hoffmann TJ et al. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics 50(3):401-413 (2018)
Allele C
OR
β 0.083
p 1.0e-65
N 94,674
Large GWAS
multi-ancestry
Burkhardt R et al. Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. Arteriosclerosis, Thrombosis, and Vascular Biology 28(11):2078-84 (2008)
Allele C
OR 18.00
p 1.0e-8
N 2,346
Large GWAS
Oceanian

total cholesterol measurement

Hoffmann TJ et al. A large electronic-health-record-based genome-wide study of serum lipids. Nature Genetics 50(3):401-413 (2018)
Allele C
OR
β 0.075
p 4.0e-57
N 94,674
Large GWAS
multi-ancestry

This variant is in our database but has no known associations or PRS memberships yet.

Gene information from NCBI Gene. Variant classifications from ClinVar.

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