This comprehensive test examines both the BRCA1 and BRCA2 genes for mutations and large deletions or duplications that may contribute to an increased risk of hereditary cancers. It is recommended for individuals with a strong family history of cancer or those meeting clinical criteria for genetic testing. The test provides critical insights for risk assessment, preventive strategies, and tailored treatment plans, helping individuals and healthcare providers make informed decisions about surveillance, lifestyle changes, and possible preventive interventions.