Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

SLCO1B1

solute carrier organic anion transporter family member 1B1

Chromosome
12
Cytoband
12p12.1
Variants (rsID)
108

SLCO1B1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12p12.1). Its official name is “solute carrier organic anion transporter family member 1B1”. The reference table lists 108 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

10 reference-table entries with clinical significance.

  • rs11045852Benignsingle nucleotide variantRotor syndrome
  • rs2306283Benignsingle nucleotide variantRotor syndrome|Gilbert syndrome
  • rs34671512Benignsingle nucleotide variantRotor syndrome
  • rs4149057Benignsingle nucleotide variantRotor syndrome
  • rs4149087Benignsingle nucleotide variantRotor syndrome
  • rs59113707Benignsingle nucleotide variantRotor syndrome
  • rs71581941Conflicting interpretationssingle nucleotide variantRotor syndrome
  • rs77271279Conflicting interpretationssingle nucleotide variantRotor syndrome
  • rs4149056Drug responsesingle nucleotide variantRotor syndrome|simvastatin acid response - Metabolism/PK|Gilbert syndrome|simvastatin response - Toxicity|hmg coa reductase inhibitors response - Toxicity|atorvastatin response - Toxicity|rosuvastatin response - Metabolism/PK|atorvastatin response - Metabolism/PK
  • rs59502379Likely benignsingle nucleotide variantRotor syndrome

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.