Lynch Syndrome HNPCC Syndrome

TEST CODE MG00350
TEST NAME Lynch Syndrome HNPCC Syndrome
RELATED GENE PMS2
SYNONYMOUS PMS2
OMIM 600259
HEREDITY
CLINICAL AREA Lynch Syndrome HNPCC Syndrome is an autosomal dominantly inherited disease. Mutations in the PMS2 gene have been associated with the disease.
METHOD Next Generation Sequencing
SAMPLE TYPE Blood with EDTA
QUANTITY 3 mL
TAT 40 DAYS

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