GTR Home > Tests > Non-Syndromic Hearing Loss Panel

Overview

Test order codeHelp: EA0201

Test name

Help

Non-Syndromic Hearing Loss Panel

Purpose of the test

Help

This is a clinical test intended for Help: Diagnosis

Condition

Help

2 conditions tested. Click Indication tab for more information.

Methodology

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

Summary of what is tested

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

Genes

Clinical validity

Help

Not provided

Clinical utility

Help

Not provided

How to order

Help

Choose the preferred way to order: 1) Online ordering: place the order in Nucleus. 2) PDF ordering: download a form, fill in and mail. 3) Sample kit: use Blueprint Kit with sample tube, requisition form and prepaid return.
Order URL Help: http://blueprintgenetics.com/order/how-to-order/

Test services

Help
  • Clinical Testing/Confirmation of Mutations Identified Previously

Practice guidelines

  • ACMG, 2002
    Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss

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.

Support Center