How should we address the inevitable harms from non‐negligent variant reclassification in predictive genetic testing?

The process of interpreting genetic variants, in which experts use all available evidence to determine whether an identified variant is associated with a current or future disease, is both scientific and nevertheless subjective. In this paper, we summarize the existing evidence that any given varian...

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Detalles Bibliográficos
Autores principales: Rashkin, Misha, Kingham, Kerry, Lara‐Otero, Karlena, Mckenna, Meghan, Villiers, Janelle, Worthington, Monty Mykolas, Prince, Anya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Professional Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092710/
https://www.ncbi.nlm.nih.gov/pubmed/36260514
http://dx.doi.org/10.1002/jgc4.1638

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092710/
https://www.ncbi.nlm.nih.gov/pubmed/36260514
http://dx.doi.org/10.1002/jgc4.1638

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