An analysis of allele, genotype and phenotype frequencies, actionable pharmacogenomic (PGx) variants and phenoconversion in 5408 Australian patients genotyped for CYP2D6, CYP2C19, CYP2C9 and VKORC1 genes

Sam Mostafa1, Carl M. Kirkpatrick1, Keith Byron2, Leslie J. Sheffield3
1Centre for Medicine Use and Safety, Monash University, Parkville, VIC, Australia
2Australian Clinical Labs, Clayton, VIC, Australia
3MyDNA Life, Australia Limited, South Yarra, VIC, Australia

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