What does the Hereditary Cancer Risk Panel + Counselling involve?

This service uses next-generation sequencing (NGS) to analyze over 50 genes associated with hereditary cancer syndromes, such as BRCA1/2, Lynch syndrome genes, and others. A simple blood or saliva sample is collected, and results are processed within approximately four weeks. After the report is ready, you will have a one-on-one session with a certified genetic counsellor who explains your results, assesses your personal and family cancer risk, and provides guidance on screening or preventive measures. The entire process is non-invasive and does not require any special preparation.