Service Providers for MSH6
MSH6 (MutS Homolog 6) is a gene that plays a critical role in the DNA mismatch repair system, helping to identify and correct errors during DNA replication. Mutations in MSH6 are linked to Lynch syndrome (hereditary nonpolyposis colorectal cancer, or HNPCC), a genetic condition that increases the risk of various cancers, including colorectal, endometrial, and ovarian cancers. Genetic testing for MSH6 mutations can help diagnose Lynch syndrome, enabling early cancer surveillance and prevention for affected individuals and their families. The test typically involves analyzing a blood or tissue sample. Identifying MSH6 mutations aids in managing cancer risk through enhanced screening and preventive strategies.