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TTN Gene Cardiomyopathy, familial hypertrophic type 9 NGS Genetic Test

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TTN Gene Cardiomyopathy, familial hypertrophic type 9 NGS Genetic Test

Short Name: TTN Cardiomyopathy NGS Test

Also known as: TTN Gene Test for Cardiomyopathy, Familial Hypertrophic Cardiomyopathy Type 9 Genetic Test, Titin Gene Mutation Analysis

TTN Gene Cardiomyopathy, familial hypertrophic type 9 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 3-4 weeks. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect mutations in the TTN gene associated with familial hypertrophic cardiomyopathy type 9, aiding in diagnosis, risk assessment, and management of the condition.

Test Code
5237
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3-4 weeks
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

Provide detailed clinical history and undergo a genetic counseling session to draw a pedigree chart of affected family members.

Method: Venipuncture or Finger prick

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or finger prick, or saliva sample if applicable.

Step 3

Report Delivery

Sample is processed and sent to the laboratory for NGS analysis.

Timeline: 3-4 weeks

Patient Instructions

1
Before the Test:Genetic counseling session and clinical history assessment to determine test necessity.
2
During the Test:Sample collection and processing in the laboratory using NGS technology.
3
After the Test:Report generation, delivery, and follow-up consultation with a genetic counselor or physician.

About This Test

Who Should Get This Test

To detect mutations in the TTN gene associated with familial hypertrophic cardiomyopathy type 9, aiding in diagnosis, risk assessment, and management of the condition.

How to Prepare

  • Fast for 8-12 hours if required, though not mandatory for this test
  • Avoid strenuous activity before sample collection
  • Bring identification and referral documents

Doctor's Notes

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

"Genetic testing for TTN mutations is crucial for early diagnosis and management of familial hypertrophic cardiomyopathy, especially in families with a history of cardiac issues."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs per requirement
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or Finger prick

Sample Stability

Blood samples stable at room temperature for 24 hours
Extracted DNA stable at -20°C for long-term storage
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Insufficient sample volume
  • Improperly labeled containers

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the TTN gene, which are associated with familial hypertrophic cardiomyopathy type 9.
📊

Positive for pathogenic mutation

Confirms genetic predisposition to FHC type 9; recommend clinical evaluation and family screening.

📊

Negative for pathogenic mutation

No known mutations detected; does not rule out other causes of cardiomyopathy.

📊

Variant of uncertain significance (VUS)

Further testing and clinical correlation needed; genetic counseling advised.

⚠️ When to Consult a Doctor:

If you experience symptoms like chest pain, shortness of breath, or have a family history of cardiomyopathy, consult a cardiologist or genetic specialist for evaluation.

Limitations

  • May not detect all genetic variants or novel mutations
  • Results require interpretation by a genetic counselor or specialist
  • Does not replace clinical diagnosis; should be used alongside other tests

Risks & Considerations

  • Minimal risks from blood draw, such as bruising, swelling, or infection
  • Psychological impact of genetic results; counseling provided

Interfering Factors

  • Poor sample quality or contamination
  • Hemolyzed blood samples
  • Insufficient DNA quantity

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ComparisonTTN Gene Cardiomyopathy, familial hypertrophic type 9 NGS Genetic Test

Frequently Asked Questions

What is TTN gene cardiomyopathy?
TTN gene cardiomyopathy is a type of familial hypertrophic cardiomyopathy caused by mutations in the TTN gene, which affects the titin protein in heart muscle cells.
How is the NGS genetic test performed?
The test uses next-generation sequencing to analyze DNA from a blood or saliva sample, detecting mutations in the TTN gene.
What does a positive test result mean?
A positive result indicates a pathogenic mutation in the TTN gene, increasing the risk for familial hypertrophic cardiomyopathy type 9.
Is genetic counseling required before the test?
Yes, a genetic counseling session is recommended to discuss implications, draw a family pedigree, and interpret results.
How long does it take to get the test results?
Results are typically available within 3-4 weeks after sample collection.
Is the test covered by insurance?
Coverage varies; it is not typically covered under government schemes like PMJAY, but check with private insurers.
Can children undergo this genetic test?
Yes, the test can be performed on individuals of all ages, but parental consent and counseling are advised for minors.
What are the risks of the test?
Risks are minimal, primarily related to blood draw, such as bruising or infection. Psychological risks are addressed through counseling.
How accurate is the NGS genetic test?
NGS technology is highly accurate for detecting known mutations, but may not identify all variants; results should be clinically correlated.
What should I do after receiving the test results?
Consult a healthcare professional or genetic counselor to discuss results, management options, and family screening.
Is home sample collection available for this test?
Yes, free home sample collection is offered for online bookings across India.
How can I book the TTN gene cardiomyopathy test?
You can book online through DNA Labs India's website or contact their customer service for assistance.
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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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.

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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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