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Laboratory: Genomics
Test Name:
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY (FHC, HCM) - MYBPC3 GENE - (B)
Test Code: MD
Clinical Information:
Only one mutation, InsG791, in the MYBPC3 gene is tested for.  This mutation is found in the Manitoba Mennonite population.
Collection Devices:
Specimen Required:
Blood: 8.0 mL
Pediatric Blood: 3.0 mL

Specimen must be kept at room temperature. Pediatric volume for infants only.
Referral:
Requisition:
Reference Values:
An interpretive report will be sent.
Availability:
Within 8 Weeks
See Also:
More Information:
Do NOT centrifuge.  Specimen is forwarded to Health Sciences Centre - MS5 for analysis.  Store and ship specimens at room temperature.  Specimens sent for Molecular tests are not to be used for other tests (ie. CBC).