Lynch Syndrome Panel Test code: 01702 • 10–21 days turnaround time Analyzes genes that are associated with Lynch syndrome. 21 genes

$0.00

Lynch Syndrome Panel                              21 genes

This panel analyzes genes associated with Lynch syndrome and constitutional mismatch repair deficiency syndrome (CMMR-D), two inherited conditions associated with an increased risk of developing certain cancers.

Genetic testing can provide valuable information by helping to:

  • Confirm or clarify a clinical diagnosis

  • Identify an inherited cancer predisposition

  • Assess potential cancer risk

  • Support appropriate cancer screening and surveillance

  • Help inform disease prognosis and progression

  • Facilitate earlier detection of cancer or related symptoms

  • Inform family planning and genetic counseling

  • Identify potentially affected relatives who may benefit from genetic testing

  • Support consideration for relevant clinical trials

Identifying a disease-causing genetic variant may help patients and healthcare professionals develop an appropriate medical management and surveillance plan based on the individual's hereditary cancer risk.

Important Testing Information:
This panel is specifically designed to identify heritable germline genetic variants. It is not intended to detect somatic mutations in tumor tissue and should not be used as a substitute for tumor-based somatic testing.