Skip to main content
DNA Labs India

TNNI3 Gene Cardiomyopathy, dilated type 2A NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

TNNI3 Gene Cardiomyopathy, dilated type 2A NGS Genetic Test

Also known as: Dilated Cardiomyopathy Type 2A, TNNI3 Cardiomyopathy

TNNI3 Gene Cardiomyopathy, dilated type 2A 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.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose TNNI3 gene mutations causing dilated cardiomyopathy type 2A, aiding in clinical management and family screening.

Test Code
2516
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
Step 1

Sample Collection

Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with TNNI3 gene cardiomyopathy.

Step 2

Laboratory Analysis

Your sample is analyzed using NGS Technology in our laboratory.

Step 3

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

Patient Instructions

1
Before the Test:Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with TNNI3 gene cardiomyopathy.

About This Test

Who Should Get This Test

To diagnose TNNI3 gene mutations causing dilated cardiomyopathy type 2A, aiding in clinical management and family screening.

How to Prepare

  • Provide a blood sample or extracted DNA
  • For FTA card, one drop of blood is sufficient

Doctor's Notes

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

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card

Understanding Your Results

Results indicate the presence or absence of mutations in the TNNI3 gene associated with dilated cardiomyopathy type 2A.
📊

Positive for pathogenic variant

Confirms diagnosis of TNNI3 gene cardiomyopathy. Genetic counseling and family screening recommended.

📊

Negative

No pathogenic variants detected. Clinical correlation advised.

⚠️ When to Consult a Doctor:

If you experience symptoms of heart failure or have a family history of cardiomyopathy, consult a cardiologist or geneticist.

Risks & Considerations

  • Minor bruising at blood draw site
  • Rare infection risk

Frequently Asked Questions

What is TNNI3 gene cardiomyopathy?
TNNI3 gene cardiomyopathy is an inherited condition caused by mutations in the TNNI3 gene, leading to dilated cardiomyopathy type 2A, where the heart muscle becomes weak and enlarged.
What are the symptoms of dilated cardiomyopathy type 2A?
Symptoms may include shortness of breath, fatigue, swelling in legs and ankles, irregular heartbeat, chest pain, and fainting.
How is TNNI3 gene cardiomyopathy diagnosed?
Diagnosis involves genetic testing, such as the NGS Genetic Test, to identify mutations in the TNNI3 gene from a blood sample.
What is NGS genetic testing?
NGS (Next-Generation Sequencing) is a technology that analyzes multiple genes simultaneously, providing comprehensive DNA analysis for accurate mutation detection.
What is the cost of the TNNI3 gene cardiomyopathy NGS test?
The test costs INR 20,000 at DNA Labs India, with free home sample collection available across India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test in numerous cities across India.
What treatment options are available?
Treatment focuses on managing symptoms with medications like beta-blockers or ACE inhibitors, and in severe cases, heart transplant may be considered.
Is genetic counseling recommended?
Yes, genetic counseling is recommended for affected individuals and family members to understand risks and implications.
Can family members be tested?
Yes, family members at risk may benefit from genetic testing to identify mutations early and guide preventive measures.
What are the risks of the test?
Risks are minimal and may include minor bruising at the blood draw site or rare infection risk.
How accurate is the NGS genetic test?
NGS genetic testing is highly accurate for detecting mutations in the TNNI3 gene, aiding in precise diagnosis.
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.

Related Tests

For Hospitals & Clinics

Reference 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.

LIMS Integration

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.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.