Service Providers for MLH1
MLH1 (MutL Homolog 1) is a gene that plays a crucial role in the repair of DNA mismatches during cell division. Mutations in MLH1 are associated with Lynch syndrome (also known as hereditary nonpolyposis colorectal cancer, or HNPCC), a genetic condition that increases the risk of colorectal, endometrial, and other cancers. Testing for MLH1 mutations can help diagnose Lynch syndrome and guide cancer screening and prevention strategies for affected individuals and their families. The test is typically performed through genetic testing of a blood or tissue sample. Identifying MLH1 mutations helps in managing cancer risk and determining appropriate surveillance or treatment plans.