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  • Molecular assay reagents intended to identify deletions or duplications of the UDP glucuronosyltransferase family 1 member A1 (UGT1A1) gene, located at chromosome 2q37.1, which encodes the protein UDP-glucuronosyltransferase 1-1. Genetic variants at this locus have been associated with Crigler-Najjar syndrome, Lucey-Driscoll syndrome, Gilbert syndrome, and altered response to various pharmaceuticals.
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