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TGFB3 Gene Arrhythmogenic right ventricular cardiomyopathy type 1 NGS Genetic Test

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TGFB3 Gene Arrhythmogenic right ventricular cardiomyopathy type 1 NGS Genetic Test

Also known as: ARVC1, Arrhythmogenic Right Ventricular Cardiomyopathy Type 1

TGFB3 Gene Arrhythmogenic right ventricular cardiomyopathy type 1 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next Generation Sequencing (NGS) 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

The purpose of the TGFB3 Gene NGS Genetic Test is to identify mutations in the TGFB3 gene that cause Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 (ARVC1). This aids in accurate diagnosis, risk stratification, family planning, and tailored treatment strategies to prevent complications such as arrhythmias and sudden cardiac death.

Test Code
2496
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
Next Generation Sequencing (NGS)
Step 1

Sample Collection

No special preparation required. Ensure proper identification and consent. For blood samples, avoid excessive physical activity prior to collection.

Method: Venipuncture or saliva collection

Step 2

Laboratory Analysis

Blood draw via venipuncture or saliva collection using a provided kit. Minimal discomfort expected.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Resume normal activities unless advised otherwise.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:No fasting required. Provide clinical history and undergo genetic counseling for pedigree analysis.
2
During the Test:Sample collection via blood draw or saliva; procedure takes about 10-15 minutes.
3
After the Test:Results available in 3-4 weeks. Follow-up with genetic counselor recommended.

About This Test

Who Should Get This Test

The purpose of the TGFB3 Gene NGS Genetic Test is to identify mutations in the TGFB3 gene that cause Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 (ARVC1). This aids in accurate diagnosis, risk stratification, family planning, and tailored treatment strategies to prevent complications such as arrhythmias and sudden cardiac death.

How to Prepare

  • Use sterile equipment for blood collection
  • For saliva, avoid eating or drinking 30 minutes prior
  • Label samples correctly with patient details
  • Store at ambient room temperature as specified

Doctor's Notes

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

"Early genetic testing for TGFB3 mutations is crucial for risk assessment, family screening, and personalized management of Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 to prevent sudden cardiac events."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture or saliva collection

Sample Stability

Blood samples: Stable for 7 days at room temperature
Extracted DNA: Stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Incorrect labeling or missing documentation

Understanding Your Results

Results from the TGFB3 Gene NGS Genetic Test indicate the presence or absence of mutations in the TGFB3 gene. Positive results confirm genetic predisposition to ARVC1, while negative results suggest no known pathogenic variants, though clinical correlation is essential.
📊

Positive for pathogenic variant

Confirms diagnosis of ARVC1 due to TGFB3 mutation. Recommend cardiac monitoring, family screening, and management by a cardiologist.

📊

Negative for pathogenic variant

No TGFB3 mutations detected. ARVC1 may still be possible due to other genes or clinical factors; further evaluation needed.

📊

Variant of uncertain significance (VUS)

Genetic change detected but clinical significance unknown. Requires periodic re-evaluation and genetic counseling.

⚠️ When to Consult a Doctor:

Consult a cardiologist or genetic specialist if you experience symptoms like palpitations, fainting, or chest pain, or if you have a family history of ARVC1. After testing, discuss results with a healthcare provider for appropriate management.

Limitations

  • Test may not detect all genetic variants due to technical limitations
  • Results require interpretation by a genetic counselor or specialist
  • Does not rule out other causes of cardiomyopathy

Risks & Considerations

  • Minor bruising or discomfort at blood draw site
  • Emotional impact of genetic results
  • Risk of false positives or negatives, though rare with NGS

Interfering Factors

  • Contaminated or degraded DNA samples
  • Recent blood transfusions may affect results
  • Technical errors in sample handling or sequencing

Frequently Asked Questions

What is Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 (ARVC1)?
ARVC1 is a rare genetic heart disorder where heart muscle is replaced by fatty or fibrous tissue, leading to arrhythmias and risk of sudden cardiac arrest, often caused by TGFB3 gene mutations.
What does the TGFB3 Gene NGS Genetic Test detect?
This test uses Next Generation Sequencing to identify mutations in the TGFB3 gene associated with ARVC1, helping in diagnosis and risk assessment.
Who should consider this genetic test?
Individuals with symptoms of ARVC1, family history of the condition, or abnormal cardiac findings should consider testing for early detection and management.
How is the test performed?
The test analyzes DNA from a blood or saliva sample using NGS technology. Sample collection is simple and can be done at home or a lab.
What is the cost of the TGFB3 Gene NGS Genetic Test?
The test costs INR 20000 at DNA Labs India, with free home sample collection available across many cities in India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection, delivered via online portal, email, or WhatsApp.
Is fasting required before the test?
No, fasting is not required. You can eat and drink normally before sample collection.
What do positive results mean?
Positive results indicate a pathogenic mutation in the TGFB3 gene, confirming genetic predisposition to ARVC1. Consult a cardiologist for management options.
Can this test be used for family screening?
Yes, if a mutation is identified, family members can be tested to assess their risk and enable early intervention.
Are there any risks associated with the test?
Risks are minimal, such as slight discomfort during blood draw. Genetic results may have emotional implications, so counseling is recommended.
Is the test covered by insurance?
Coverage varies by insurance plan. Check with your provider; schemes like PMJAY or CGHS may not cover it, but private insurance might.
How accurate is the TGFB3 Gene NGS Genetic Test?
NGS technology is highly accurate for detecting genetic mutations, but results should be interpreted by a specialist in the context of clinical symptoms.
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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