rs73079476

This is a intron variant variant in the SLCO1B1 gene.

GWAS Catalog Trait Associations (33)

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

1-linoleoyl-GPG (18:2) measurement

Allele C
OR 0.39
p 5.0e-52
N 6,136
Large GWAS
European

deoxycholic acid glucuronide measurement

Allele C
OR 0.34
p 9.0e-45
N 6,136
Large GWAS
European

X-17653 measurement

Allele C
OR 0.32
p 6.0e-43
N 6,136
Large GWAS
European

testosterone measurement

Allele A
OR 0.05
p 4.0e-40
N 194,453
Large GWAS
European
Allele A
OR 0.04
p 2.0e-14
N 137,984
Major Consortium StudyLarge GWAS
multi-ancestry

4-androsten-3beta,17beta-diol disulfate 2 measurement

Allele A
OR 0.18
p 4.0e-35
N 14,296
Large GWAS
European

triglycerides to total lipids in very small VLDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.03
p 4.0e-35
N 450,015
Large GWAS
multi-ancestry

cholesterol to total lipids in very small VLDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.03
p 1.0e-30
N 450,015
Large GWAS
multi-ancestry

cholesteryl esters to total lipids in very small VLDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.03
p 7.0e-29
N 450,015
Large GWAS
multi-ancestry

free cholesterol to total lipids in very small VLDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.03
p 4.0e-26
N 450,015
Large GWAS
multi-ancestry

triglycerides to total lipids in IDL percentage

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele C
OR 0.03
p 6.0e-23
N 450,015
Large GWAS
multi-ancestry

About SLCO1B1

This gene encodes a liver-specific member of the organic anion transporter family. The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of numerous endogenous compounds including bilirubin, 17-beta-glucuronosyl estradiol and leukotriene C4. This protein is also involved in the removal of drug compounds such as statins, bromosulfophthalein and rifampin from the blood into the hepatocytes. Polymorphisms in the gene encoding this protein are associated with impaired transporter function. [provided by RefSeq, Mar 2009]

View all SLCO1B1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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