GTR Home > Tests > Brugada syndrome

Overview

Test name

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Brugada syndrome

Purpose of the test

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This is a clinical test intended for Help: Diagnosis, Pre-symptomatic, Therapeutic management

Condition

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8 conditions tested. Click Indication tab for more information.

Methodology

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Molecular Genetics
DDeletion/duplication analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
CSequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)

Summary of what is tested

10 genes and variants. Click Methodology tab for more information.

Genes

Clinical validity

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Not provided

Clinical utility

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Not provided

Testing strategy

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Full gene sequencing and deletion/duplication analysis of targeted genes

How to order

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Tests can be ordered online or by submitting a paper requisition form.
Order URL Help: https://www.invitae.com/ordering

Test services

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  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Genetic counseling

Clinical resources

Practice guidelines

  • HRS/EHRA/APHRS, 2013
    Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.
  • AHRQ, 2013
    Assessment on Implantable Defibrillators and the Evidence for Primary Prevention of Sudden Cardiac Death

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.