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  • Molecular assay reagents intended to identify mutations in the solute carrier organic anion transporter family member 1B1 (SLCO1B1) gene, located at chromosome 12p12.1, which encodes the protein solute carrier organic anion transporter family member 1B1. Genetic variants at this locus have been associated with altered response to simvastatin, statin-induced myopathy, and Rotor syndrome.
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