rs12318075

This is a intron variant variant in the SLCO1B1 gene.

GWAS Catalog Trait Associations (8)

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

X-21467 measurement

Allele G
OR 0.43
p 2.0e-100
N 8,195
Large GWAS
European

metabolite measurement

Allele G
OR 0.35
p 4.0e-67
N 7,861
Large GWAS
European

glycolithocholate sulfate measurement

Allele T
OR 0.23
p 1.0e-60
N 14,296
Large GWAS
European

X-25433 measurement

Allele G
OR 0.35
p 8.0e-56
N 6,516
Large GWAS
European

X-21471 measurement

Allele G
OR 0.31
p 6.0e-32
N 3,964
Large GWAS
European

isoursodeoxycholate sulfate (2) measurement

Feofanova EV et al. Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations. Nature Communications 14(1):3111 (2023)
Allele G
OR 0.38
p 4.0e-19
N 1,832
Large GWAS
multi-ancestry

1-palmitoyl-GPG (16:0) measurement

Allele G
OR 0.13
p 4.0e-15
N 4,885
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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