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GJB3 Gene Deafness, autosomal dominant type 2B NGS Genetic Test

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GJB3 Gene Deafness, autosomal dominant type 2B NGS Genetic Test

Short Name: GJB3 Deafness Type 2B NGS Test

Also known as: DFNA2B, GJB3-related hearing loss

GJB3 Gene Deafness, autosomal dominant type 2B NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in Results are typically available within 3 to 4 weeks after sample collection.. Free home collection in 300+ cities across India.

NGS Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect pathogenic mutations in the GJB3 gene that cause autosomal dominant deafness type 2B, aiding in diagnosis, management, and genetic counseling for affected individuals and families.

Test Code
2306
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
Results are typically available within 3 to 4 weeks after sample collection.
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No specific preparation is required. Genetic counseling is recommended to discuss test implications and draw a family pedigree chart.

Method: Blood draw or saliva collection

Step 2

Laboratory Analysis

A small blood sample or saliva will be collected by a trained phlebotomist; the process is simple and painless.

Step 3

Report Delivery

Apply pressure to the puncture site for a few minutes if blood was drawn. No specific restrictions after collection.

Timeline: Results are typically available within 3 to 4 weeks after sample collection.

Patient Instructions

1
Before the Test:Genetic counseling session to discuss test implications, draw a family pedigree chart, and obtain informed consent.
2
During the Test:Simple blood draw or saliva collection; the process takes about 10-15 minutes with minimal discomfort.
3
After the Test:Sample sent to the laboratory for NGS analysis; results are delivered within 3-4 weeks via online portal, email, or WhatsApp.

About This Test

Who Should Get This Test

To detect pathogenic mutations in the GJB3 gene that cause autosomal dominant deafness type 2B, aiding in diagnosis, management, and genetic counseling for affected individuals and families.

How to Prepare

  • No fasting required
  • Bring a valid ID and prescription if available
  • Inform the technician about any blood-thinning medications or health conditions

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Genetic testing for GJB3 mutations is essential for identifying the cause of autosomal dominant hearing loss, enabling early intervention, management, and family counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5 mL blood or equivalent
ContainerEDTA tube for blood
Collection MethodBlood draw or saliva collection

Sample Stability

Blood at room temperature
Saliva
Sample Rejection Criteria:
  • Insufficient sample volume
  • Hemolyzed or clotted samples
  • Improperly labeled or contaminated samples

Understanding Your Results

The test results will indicate the presence or absence of pathogenic mutations in the GJB3 gene, which are associated with autosomal dominant deafness type 2B.
📊

Diagnosis of GJB3-related autosomal dominant deafness is supported. Genetic counseling and management plans should be initiated, including hearing assessments and family testing.

📊

Further testing, family studies, or functional assays may be needed. Consult a geneticist for clarification and monitoring.

📊

GJB3-related deafness is unlikely, and other genetic or non-genetic causes of hearing loss should be explored through additional evaluations.

⚠️ When to Consult a Doctor:

If you have a family history of hearing loss, experience progressive hearing loss, or have unexplained hearing impairment, consult a geneticist or ENT specialist for evaluation and testing recommendations.

Limitations

  • May not detect all genetic variants
  • Not a diagnostic for all causes of hearing loss
  • Results require genetic counseling for interpretation

Risks & Considerations

  • Minimal risk from blood draw (e.g., bruising, infection)
  • Psychological impact of test results, such as anxiety
  • Possible detection of incidental findings not related to deafness

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Hemolyzed blood samples

Compare With Similar Tests

TestGJB3 Gene Deafness, autosomal dominant type 2B NGS Genetic TestGJB2 Gene Deafness TestSLC26A4 Gene TestTMC1 Gene TestComprehensive Hearing Loss Panel
ComparisonGJB3 Gene Deafness, autosomal dominant type 2B NGS Genetic Test

Frequently Asked Questions

What is the GJB3 gene deafness test?
The GJB3 gene deafness test is an NGS genetic test that analyzes the GJB3 gene to identify mutations associated with autosomal dominant deafness type 2B, helping diagnose hereditary hearing loss.
Who should get tested for GJB3 gene mutations?
Individuals with a family history of hearing loss, progressive hearing impairment, tinnitus, or unexplained deafness should consider testing, especially if symptoms align with autosomal dominant patterns.
How is the test performed?
The test involves collecting a small blood sample or saliva, which is then analyzed in the laboratory using Next-Generation Sequencing (NGS) technology to detect mutations in the GJB3 gene.
What does the test cost at DNA Labs India?
The GJB3 Gene Deafness NGS Genetic Test costs INR 20,000, which includes sample collection, laboratory analysis, and a detailed report. Home collection is free for online bookings.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection for online bookings across India, making it convenient for patients to get tested without visiting a clinic.
How long does it take to get the results?
Results are typically available within 3 to 4 weeks after sample collection. They can be accessed via online portal, email, or WhatsApp.
What are the symptoms of GJB3 gene deafness?
Symptoms include progressive hearing loss, tinnitus, difficulty understanding speech in noisy environments, dizziness, vertigo, and a feeling of fullness or pressure in the ears.
Is genetic counseling necessary before testing?
Yes, genetic counseling is recommended before testing to discuss the implications, understand the test process, and draw a family pedigree chart for accurate interpretation.
Can the test be done on children?
Yes, the test can be performed on individuals of all ages, including children, if there is suspicion of GJB3-related hearing loss. Parental consent is required for minors.
What if a pathogenic variant is found in the test?
If a pathogenic variant is detected, it supports a diagnosis of GJB3-related deafness. Genetic counseling will guide further management, including hearing interventions and family testing.
How accurate is the NGS genetic test for GJB3 mutations?
NGS technology provides high accuracy for detecting mutations in the GJB3 gene, but no test is 100% infallible. Results should be interpreted by a geneticist in clinical context.
Is the test covered by insurance in India?
Coverage varies by insurance provider. It is not typically covered under government schemes like PMJAY or CGHS, but private insurance may offer some coverage. Check with your insurer for details.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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