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Lynch Syndrome (MSH6) Full Gene Analysis Prior Authorization Ordering Instructions Mayo Clinic Laboratories is pleased to offer prior authorization services and third party billing on our MSH6 Gene,
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Lynch syndrome MSH6 full refers to a genetic test that identifies mutations in the MSH6 gene associated with Lynch syndrome, a hereditary condition that increases the risk of certain types of cancers.
Individuals with a family history of Lynch syndrome or a personal history of Lynch syndrome-related cancers may be required to undergo Lynch syndrome MSH6 full testing.
The Lynch syndrome MSH6 full test is typically administered by a healthcare provider who will collect a sample, analyze it for mutations, and provide the results to the individual.
The purpose of Lynch syndrome MSH6 full testing is to identify individuals at risk for Lynch syndrome and provide them with appropriate medical management and genetic counseling.
The Lynch syndrome MSH6 full report typically includes information about the specific MSH6 gene mutations identified, as well as recommendations for surveillance and prevention of Lynch syndrome-associated cancers.
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