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.
GWAS Catalog Trait Associations (10)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
bilirubin measurement
X-21339 measurement
pregnenediol disulfate (C21H34O8S2) measurement
tyrosine measurement
allopregnanolone sulfate measurement, pregnanolone sulfate measurement
21-hydroxypregnenolone disulfate measurement
androstenediol (3beta,17beta) disulfate (2) measurement
mean corpuscular hemoglobin concentration
heel bone mineral density
urate measurement
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.
Community Wiki
No community notes yet for this variant. Sign in to start one.
Comments
Sign in to join the discussion.
Loading comments…