rs4149083

This is a intron variant variant in the SLCO1B1 gene.

GWAS Catalog Trait Associations (10)

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

bilirubin measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.15
p
N 467,170
Large GWAS
multi-ancestry
Allele T
OR 0.18
p 2.0e-18
N 8,809
Large GWAS
European

X-21339 measurement

Allele T
OR 0.20
p 8.0e-23
N 8,203
Large GWAS
European

pregnenediol disulfate (C21H34O8S2) 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 0.20
p 4.0e-19
N 9,016
Large GWAS
multi-ancestry

tyrosine measurement

Karjalainen MK et al. Genome-wide characterization of circulating metabolic biomarkers. Nature 628(8006):130-138 (2024)
Allele A
OR 0.05
p 6.0e-18
N 136,016
Large GWAS
multi-ancestry

mean corpuscular hemoglobin concentration

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.03
p 3.0e-13
N 583,935
Major Consortium StudyLarge GWAS
multi-ancestry

heel bone mineral density

Morris JA et al. An atlas of genetic influences on osteoporosis in humans and mice. Nature Genetics 51(2):258-266 (2019)
Allele A
OR 0.02
p 1.0e-12
N 426,824
Large GWAS
European

urate measurement

Cho C et al. Large-scale cross-ancestry genome-wide meta-analysis of serum urate. Nature Communications 15(1):3441 (2024)
Allele A
OR 0.02
p 1.0e-8
N 677,373
Meta-analysisLarge 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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