MYO15A Gene Deafness, autosomal recessive type 3 NGS Genetic Test
Short Name: MYO15A Genetic Test
Also known as: DFNB3, MYO15A-related hearing loss
MYO15A Gene Deafness, autosomal recessive type 3 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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
To identify mutations in the MYO15A gene responsible for autosomal recessive deafness type 3, aiding in diagnosis, management, and genetic counseling.
- Test Code
- 2335
- 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 Technology
Sample Collection
No specific preparation required. Provide clinical history and undergo genetic counseling.
Method: Venipuncture or fingerstick
Laboratory Analysis
Blood sample collected via venipuncture or fingerstick for FTA card.
Report Delivery
Apply pressure to the puncture site. Store sample as instructed.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the MYO15A gene responsible for autosomal recessive deafness type 3, aiding in diagnosis, management, and genetic counseling.
How to Prepare
- Use EDTA tube for blood or FTA card for one drop blood
- Label sample with patient details
- Transport at ambient room temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for MYO15A is crucial for diagnosing autosomal recessive deafness type 3, enabling targeted management and family counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted blood sample
- Insufficient sample volume
- Improper labeling or storage
Understanding Your Results
Consult an ENT specialist or geneticist if you have persistent hearing loss, family history of deafness, or after receiving test results for management guidance.
Limitations
- ⚠May not detect all genetic variants or large deletions
- ⚠Results require clinical correlation and genetic counseling
- ⚠Not a standalone diagnostic for all causes of deafness
Risks & Considerations
- ●Minimal risks from blood draw: bruising, infection at puncture site
Interfering Factors
- ●Contaminated or degraded DNA sample
- ●Insufficient sample volume
- ●Technical errors during NGS processing
Compare With Similar Tests
| Test | MYO15A Gene Deafness, autosomal recessive type 3 NGS Genetic Test | GJB2 Gene Test | SLC26A4 Gene Test | TECTA Gene Test | Comprehensive Deafness Panel |
|---|---|---|---|---|---|
| Comparison | MYO15A Gene Deafness, autosomal recessive type 3 NGS Genetic Test |
Frequently Asked Questions
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₹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.
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