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Cytochrome P450 family 2 subfamily D member 6 (CYP2D6) is an enzyme primarily expressed in the liver that metabolizes approximately 20-25% of clinically used drugs. Genetic variations in the *CYP2D6* gene can result in significant inter-individual differences in drug metabolism rates, leading to poor, intermediate, extensive, or ultrarapid metabolizer phenotypes. These differences can affect drug efficacy and toxicity.
Hydroxylation, demethylation, and dealkylation of various drugs and endogenous compounds.
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