Characterization of Reference Materials with an Association for Molecular Pathology Pharmacogenetics Working Group Tier 2 Status: CYP2C9, CYP2C19, VKORC1, CYP2C Cluster Variant, and GGCX: A GeT-RM Collaborative Project

dc.contributor.authorPratt, Victoria M.
dc.contributor.authorTurner, Amy
dc.contributor.authorBroeckel, Ulrich
dc.contributor.authorDawson, D. Brian
dc.contributor.authorGaedigk, Andrea
dc.contributor.authorLynnes, Ty C.
dc.contributor.authorMedeiros, Elizabeth B.
dc.contributor.authorMoyer, Ann M.
dc.contributor.authorRequesens, Deborah
dc.contributor.authorVetrini, Francesco
dc.contributor.authorKalman, Lisa V.
dc.contributor.departmentMedical and Molecular Genetics, School of Medicine
dc.date.accessioned2023-08-15T09:36:59Z
dc.date.available2023-08-15T09:36:59Z
dc.date.issued2021
dc.description.abstractPharmacogenetic testing is increasingly available from clinical and research laboratories. However, only a limited number of quality control and other reference materials are currently available for many of the variants that are tested. The Association for Molecular Pathology Pharmacogenetic Work Group has published a series of papers recommending alleles for inclusion in clinical testing. Several of the alleles were not considered for tier 1 because of a lack of reference materials. To address this need, the Division of Laboratory Systems, Centers for Disease Control and Prevention-based Genetic Testing Reference Material (GeT-RM) program, in collaboration with members of the pharmacogenetic testing and research communities and the Coriell Institute for Medical Research, has characterized 18 DNA samples derived from Coriell cell lines. DNA samples were distributed to five volunteer testing laboratories for genotyping using three commercially available and laboratory developed tests. Several tier 2 variants, including CYP2C9∗13, CYP2C19∗35, the CYP2C cluster variant (rs12777823), two variants in VKORC1 (rs61742245 and rs72547529) related to warfarin resistance, and two variants in GGCX (rs12714145 and rs11676382) related to clotting factor activation, were identified among these samples. These publicly available materials complement the pharmacogenetic reference materials previously characterized by the GeT-RM program and will support the quality assurance and quality control programs of clinical laboratories that perform pharmacogenetic testing.
dc.eprint.versionFinal published version
dc.identifier.citationPratt VM, Turner A, Broeckel U, et al. Characterization of Reference Materials with an Association for Molecular Pathology Pharmacogenetics Working Group Tier 2 Status: CYP2C9, CYP2C19, VKORC1, CYP2C Cluster Variant, and GGCX: A GeT-RM Collaborative Project. J Mol Diagn. 2021;23(8):952-958. doi:10.1016/j.jmoldx.2021.04.012
dc.identifier.urihttps://hdl.handle.net/1805/34915
dc.language.isoen_US
dc.publisherElsevier
dc.relation.isversionof10.1016/j.jmoldx.2021.04.012
dc.relation.journalThe Journal of Molecular Diagnostics
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourcePMC
dc.subjectCytochrome P-450 CYP2C19
dc.subjectPharmacogenetics
dc.subjectVitamin K Epoxide Reductases
dc.titleCharacterization of Reference Materials with an Association for Molecular Pathology Pharmacogenetics Working Group Tier 2 Status: CYP2C9, CYP2C19, VKORC1, CYP2C Cluster Variant, and GGCX: A GeT-RM Collaborative Project
dc.typeArticle
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