£1,250.00
Lynch Syndrome Detection Bundle:
This genetic testing bundle identifies mutations in MLH1, MSH2, MSH6, PMS2, and EPCAM genes linked to Lynch syndrome, a hereditary condition elevating risks for colorectal, endometrial, and ovarian cancers. Using next-generation sequencing (NGS), the panel offers precise detection of pathogenic variants. Designed for early intervention, the service enhances cancer prevention through proactive, accessible hereditary cancer care.
Access Option: In-person
Lynch Syndrome Detection Bundle:
This genetic testing bundle identifies mutations in MLH1, MSH2, MSH6, PMS2, and EPCAM genes linked to Lynch syndrome, a hereditary condition elevating risks for colorectal, endometrial, and ovarian cancers. Using next-generation sequencing (NGS), the panel offers precise detection of pathogenic variants. Designed for early intervention, the service enhances cancer prevention through proactive, accessible hereditary cancer care.
Access Option: In-person
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