rs73079476
This is a intron variant variant in the SLCO1B1 gene.
▶GWAS Catalog Trait Associations (33)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (33)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
1-linoleoyl-GPG (18:2) measurement
deoxycholic acid glucuronide measurement
X-17653 measurement
testosterone measurement
4-androsten-3beta,17beta-diol disulfate 2 measurement
triglycerides to total lipids in very small VLDL percentage
cholesterol to total lipids in very small VLDL percentage
cholesteryl esters to total lipids in very small VLDL percentage
free cholesterol to total lipids in very small VLDL percentage
triglycerides to total lipids in IDL percentage
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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