rs58310495

This variant is located in the SLCO1B1 gene.

GWAS Catalog Trait Associations (13)

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

X-12456 measurement

Allele T
OR 0.40
p 2.0e-36
N 3,214
Large GWAS
European

Eicosanodioate measurement

Allele T
OR 0.16
p 2.0e-31
N 14,296
Large GWAS
European

taurodeoxycholic acid 3-sulfate measurement

Feofanova EV et al. Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations. Nature Communications 14(1):3111 (2023)
Allele T
OR 0.47
p 3.0e-29
N 1,966
Large GWAS
multi-ancestry

metabolite measurement

Allele T
OR 0.34
p 3.0e-23
N 2,540
Large GWAS
European

eicosanedioate (C20-DC) measurement

Allele T
OR 0.17
p 1.0e-15
N 8,258
Large GWAS
European

urinary metabolite measurement

Allele T
OR 0.58
p 1.0e-15
N 1,221
Large GWAS

triglycerides in IDL measurement

Allele T
OR 0.03
p 1.0e-14
N 199,732
Large GWAS
European

gout

Major TJ et al. A genome-wide association analysis reveals new pathogenic pathways in gout. Nature Genetics 56(11):2392-2406 (2024)
Allele T
OR 0.95
p 4.0e-13
N 2,206,883
Large GWAS
European

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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