EYA4 Gene Cardiomyopathy, dilated type 1J NGS Genetic Test
Also known as: Dilated Cardiomyopathy Type 1J, EYA4-related Cardiomyopathy, DCM Type 1J
EYA4 Gene Cardiomyopathy, dilated type 1J 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 Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of the EYA4 Gene Cardiomyopathy, dilated type 1J NGS Genetic Test is to detect mutations in the EYA4 gene that cause dilated cardiomyopathy type 1J. This helps in confirming diagnosis, guiding treatment decisions, assessing risk for family members, and enabling genetic counseling.
- Test Code
- 5212
- 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
A certified phlebotomist visits your home or you visit our nearest center. The process takes under 5 minutes.
Laboratory Analysis
Your sample is analyzed using NGS Technology in our laboratory.
Report Delivery
A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.
Timeline: 3 to 4 Weeks
About This Test
Who Should Get This Test
The purpose of the EYA4 Gene Cardiomyopathy, dilated type 1J NGS Genetic Test is to detect mutations in the EYA4 gene that cause dilated cardiomyopathy type 1J. This helps in confirming diagnosis, guiding treatment decisions, assessing risk for family members, and enabling genetic counseling.
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Positive for pathogenic variant
Confirms diagnosis of EYA4 gene cardiomyopathy; genetic counseling and cardiac monitoring recommended.
Negative for pathogenic variant
No mutations detected in EYA4 gene; clinical correlation and further testing may be needed if symptoms persist.
Variant of uncertain significance
Genetic change identified but clinical significance unclear; follow-up and family studies advised.
Consult a doctor if you experience symptoms like shortness of breath, fatigue, dizziness, fainting, swelling in the legs, or irregular heartbeat, especially with a family history of heart disease. After testing, discuss results with a genetic counselor or cardiologist for appropriate management.
Limitations
- ⚠This test only detects mutations in the EYA4 gene; other genetic causes of cardiomyopathy may not be identified.
- ⚠Results may require confirmation with additional clinical evaluation.
- ⚠Genetic variants of uncertain significance may be reported.
Risks & Considerations
- ●Minimal physical risk from blood draw.
- ●Potential psychological impact from genetic results.
- ●Risk of incidental findings unrelated to cardiomyopathy.
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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