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Webinars

Complexities of variant interpretation: 3 case studies: Any Myriad publications highlighted in this webinar can be found at our publications page. If you have any specific questions, please feel free to reach out to our medical services department at helpmed@myriad.com or by dialing 800-469-7423 ext. 3850.

Reporting of TP53 mutations - Implications for genetic counseling and clinical management: Myriad has changed the way pathogenic or likely pathogenic findings in the TP53 gene are reported since additional testing is required to confirm if the findings are germline or somatic in origin. This webinar will explain Myriad’s new reporting process for pathogenic or likely pathogenic findings in TP53 and present the data that led to this change