TBC1D24 Gene Deafness, autosomal dominant type 65 NGS Genetic Test
Short Name: TBC1D24 Deafness Test
Also known as: TBC1D24 mutation test, Deafness type 65 genetic test, TBC1D24 gene sequencing
TBC1D24 Gene Deafness, autosomal dominant type 65 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS (Next-Generation Sequencing) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The purpose of this test is to detect mutations in the TBC1D24 gene that cause autosomal dominant deafness type 65, aiding in accurate diagnosis, family risk assessment, and informed medical management.
- Test Code
- 2315
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 Weeks
- Fasting Required
- No
- Method
- NGS (Next-Generation Sequencing)
Sample Collection
No specific preparation is required. Ensure genetic counseling session is scheduled if needed.
Method: Venipuncture
Laboratory Analysis
A blood sample will be drawn from a vein in your arm by a trained phlebotomist.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Resume normal activities immediately.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to detect mutations in the TBC1D24 gene that cause autosomal dominant deafness type 65, aiding in accurate diagnosis, family risk assessment, and informed medical management.
How to Prepare
- Fast for 4-6 hours if specified, though not typically required
- Bring identification and prescription if available
- Inform the technician about any medications or health conditions
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early genetic testing for TBC1D24 mutations can aid in accurate diagnosis and personalized management of hereditary deafness, potentially improving patient outcomes."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Incorrect sample type
- Labeled with incorrect patient information
Understanding Your Results
Positive
Pathogenic variant detected in TBC1D24 gene. Indicates genetic cause for deafness.
Action: Consult geneticist for counseling and management options.
Negative
No pathogenic variant detected. Deafness may be due to other genetic or non-genetic factors.
Action: Consider additional genetic tests or clinical evaluation.
Variant of Unknown Significance
A variant with uncertain clinical significance.
Action: Genetic counseling recommended for further assessment.
Consult a doctor if you experience symptoms of hearing loss, have a family history of deafness, or receive a positive test result for further evaluation and management.
Limitations
- ⚠Does not detect all genetic causes of deafness
- ⚠May not identify variants of unknown significance
- ⚠Results require correlation with clinical history
- ⚠Not suitable for prenatal diagnosis without additional validation
Risks & Considerations
- ●Minimal risk of bruising or infection at blood draw site
- ●Possible anxiety related to test results
Interfering Factors
- ●Contaminated or degraded sample
- ●Improper sample storage or handling
- ●Recent blood transfusion
- ●Presence of inhibitors in DNA extraction
Compare With Similar Tests
| Test | TBC1D24 Gene Deafness, autosomal dominant type 65 NGS Genetic Test | GJB2 Gene Test | SLC26A4 Gene Test | OTOF Gene Test | Comprehensive Deafness Panel |
|---|---|---|---|---|---|
| Comparison | TBC1D24 Gene Deafness, autosomal dominant type 65 NGS Genetic Test |
Frequently Asked Questions
What is TBC1D24 gene deafness?
How is the test performed?
Who should get tested?
What is the cost of the test?
Is home collection available?
How long does it take to get results?
What does a positive result mean?
Can this test be used for prenatal diagnosis?
Is the test covered by insurance?
Are there any risks?
How do I prepare for the test?
What if the test is negative?
Related Tests
Connexin 30 Mutation Detection Test
₹8,000COL4A3 Gene Alport syndrome, autosomal recessive NGS Genetic Test
₹20,000PLCB4 Gene Auriculocondylar syndrome type 2 NGS Genetic Test
₹20,000DIAPH3 Gene Auditory neuropathy, autosomal dominant NGS Genetic Test
₹20,000MYO7A Gene Deafness, autosomal dominant type 11 NGS Genetic Test
₹20,000POU4F3 Gene Deafness, autosomal dominant type 15 NGS Genetic Test
₹20,000Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
Book Your Test
Enter your details and we'll connect you within 15 minutes.
