Lynch Syndrome HNPCC Syndrome

TEST CODE MG00340
TEST NAME Lynch Syndrome HNPCC Syndrome
RELATED GENE PMS1
SYNONYMOUS PMS1
OMIM 600258
HEREDITY
CLINICAL AREA Lynch Syndrome HNPCC Syndrome is an autosomal dominantly inherited disease. Mutations in the PMS1 gene have been associated with the disease.
METHOD Next Generation Sequencing
SAMPLE TYPE Blood with EDTA / CVS
QUANTITY 3 mL
TAT 40 DAYS

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