Lynch Syndrome HNPCC Syndrome

TEST CODE MG00310
TEST NAME Lynch Syndrome HNPCC Syndrome
RELATED GENE MSH2
SYNONYMOUS MSH2
OMIM 120435
HEREDITY Autosomal Dominant
CLINICAL AREA Lynch Syndrome HNPCC Syndrome is an autosomal dominantly inherited disease. Mutations in the MSH2 gene have been associated with the disease.
METHOD Next Generation Sequencing
SAMPLE TYPE Blood with EDTA
QUANTITY 3 mL
TAT 40 DAYS

ORDER OPTIONS AND PRICING

Discover genetic insights at your convenience. Contact Mikrogen anytime for information on order options, pricing, and comprehensive genetic testing services