rs57743625

This variant is located in the SLCO1B1 gene.

GWAS Catalog Trait Associations (9)

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

sex hormone-binding globulin measurement

Allele G
OR 0.03
p 1.0e-159
N 368,929
Large GWAS
European

taurocholenate sulfate measurement

Allele A
OR 0.42
p 1.0e-98
N 8,249
Large GWAS
European

X-14662 measurement

Allele A
OR 0.19
p 3.0e-24
N 14,296
Large GWAS
European

X-11880 measurement

Allele A
OR 0.17
p 4.0e-18
N 8,206
Large GWAS
European

testosterone measurement

Allele A
OR 0.20
p 2.0e-17
N 148,248
Major Consortium StudyLarge GWAS
European

glycoursodeoxycholic acid sulfate (1) measurement

Allele A
OR 0.17
p 2.0e-14
N 6,622
Large GWAS
European

isthmin-1 measurement

Allele A
OR 0.05
p 6.0e-14
N 47,745
Large GWAS
European

N-oleoyltaurine measurement

Allele A
OR 0.15
p 9.0e-13
N 7,375
Large GWAS
European

taurolithocholate 3-sulfate measurement

Allele A
OR 0.14
p 3.0e-12
N 8,124
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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