Analytic Time

2 - 5 weeks

MiChart Code
Hypertrophic Cardiomyopathy Panel, Known Mutation
Soft Order Code

Test Updated:


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Test Overview

Test Methodology

A combination of oligonucleotide hybridization-based DNA sequencing using the Affymetrix GeneChip® platform and dideoxy-based DNA sequencing of the coding regions and splice sites of all genes.

Test Usage

Examines 11 genes known to cause hypertrophic cardiomyopathy (MYBPC3, MYH7, TNNT2, TNNI3, TPM1, ACTC, MYL2, MYL3, LAMP2, PRKAG2, GLA).

Reference Range

* Reference ranges may change over time. Please refer to the original patient report when evaluating results.

Specimen Requirements

Collection Onsite

Collect specimen in a lavender top (EDTA) tube. Please specify known familial mutation to be tested.

Collection Offsite

Collect specimen in a lavender top (EDTA) tube. Refrigerate and send intact specimen. Please specify known familial mutation to be tested.

Lavender Top Tube
Normal Volume
7 mL EDTA whole blood
Minimum Volume

Billing Information

CPT Code
Pro Fee Code

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Our High Standard

Quality that sets us apart

As the reference laboratory division of Michigan Medicine's Department of Pathology, MLabs shares the institution's commitment to applying established quality principles to clinical laboratory testing. Like other large organizations in complex, consequential fields, we rely on an established approach to monitor quality throughout the testing process.