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SCN5A Gene Ventricular fibrillation, paroxysmal familial type 1 NGS Genetic Test

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SCN5A Gene Ventricular fibrillation, paroxysmal familial type 1 NGS Genetic Test

Short Name: SCN5A VF Genetic Test

Also known as: SCN5A Mutation Test, Familial Ventricular Fibrillation Genetic Test, Cardiac Arrhythmia Genetic Test

SCN5A Gene Ventricular fibrillation, paroxysmal familial 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 this test is to identify mutations in the SCN5A gene associated with paroxysmal familial type 1 ventricular fibrillation, enabling accurate diagnosis, risk stratification for sudden cardiac arrest, and informed clinical management including family screening and genetic counseling.

Test Code
5301
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

Provide clinical history and undergo genetic counseling to draw a pedigree chart. No fasting required.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample will be collected via venipuncture or a drop on an FTA card by a trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Store samples as per instructions for stability.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Schedule genetic counseling, provide detailed family medical history, and ensure sample collection instructions are followed.
2
During the Test:Sample collection takes about 10-15 minutes. The process involves a simple blood draw or FTA card preparation.
3
After the Test:Results are delivered in 3-4 weeks. Follow-up with a genetic counselor or physician to discuss findings and next steps.

About This Test

Who Should Get This Test

The purpose of this test is to identify mutations in the SCN5A gene associated with paroxysmal familial type 1 ventricular fibrillation, enabling accurate diagnosis, risk stratification for sudden cardiac arrest, and informed clinical management including family screening and genetic counseling.

How to Prepare

  • Ensure proper identification and labeling of samples
  • Use sterile collection tubes
  • Transport samples at room temperature within 48 hours

Doctor's Notes

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

"This genetic test is vital for identifying hereditary risks of ventricular fibrillation, enabling early intervention and family planning counseling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume3-5 mL blood
ContainerEDTA tube or FTA card
Collection MethodVenipuncture

Sample Stability

Blood samples stable for 48 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Improper labeling or container

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the SCN5A gene. Positive results confirm genetic predisposition to ventricular fibrillation, while negative results suggest no detected mutations, but do not rule out other causes.
📊

Positive

Pathogenic variant detected, indicating high risk for familial ventricular fibrillation. Requires clinical correlation and family screening.

📊

Negative

No pathogenic variants detected. May reduce genetic risk, but clinical evaluation is still recommended.

📊

Variant of uncertain significance

Genetic variant found but clinical significance unclear. Further testing and counseling advised.

⚠️ When to Consult a Doctor:

Consult a cardiologist or genetic specialist immediately if symptoms like chest pain, palpitations, or fainting occur, or if family history suggests genetic risk.

Limitations

  • May not detect all genetic variants or non-coding region mutations
  • Results require interpretation by a genetic specialist
  • Does not replace clinical evaluation or other diagnostic tests like ECG

Risks & Considerations

  • Minimal risk from blood draw, such as slight pain, bruising, or infection at the puncture site

Interfering Factors

  • Sample contamination or degradation
  • Insufficient DNA quality or quantity
  • Technical errors in sequencing

Compare With Similar Tests

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Frequently Asked Questions

What is the SCN5A Gene Ventricular Fibrillation Test?
It is a genetic test using NGS technology to detect mutations in the SCN5A gene linked to paroxysmal familial type 1 ventricular fibrillation.
Why is this test recommended?
It is recommended for individuals with a family history of sudden cardiac arrest, unexplained syncope, or symptoms of arrhythmia to diagnose genetic causes.
How is the test performed?
A blood sample or extracted DNA is analyzed using Next Generation Sequencing to identify pathogenic variants in the SCN5A gene.
What sample is required for the test?
Blood, extracted DNA, or one drop of blood on an FTA card can be used.
Is fasting required before the test?
No, fasting is not required for this genetic test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What does a positive result mean?
A positive result indicates a pathogenic variant in the SCN5A gene, confirming genetic predisposition to ventricular fibrillation and requiring further clinical management.
What does a negative result mean?
A negative result means no pathogenic variants were detected, but it does not completely rule out other genetic or non-genetic causes.
Are there any risks associated with the test?
The test involves minimal risks from blood draw, such as slight pain or bruising. Genetic testing may have psychological implications, so counseling is advised.
Is genetic counseling provided with the test?
Yes, DNA Labs India offers a genetic counseling session before and after testing to discuss results and implications.
How much does the test cost?
The test costs INR 20,000, with free home sample collection available across India.
Is the test covered by insurance?
Coverage varies by insurance plan. It is advisable to check with your provider for specific details.
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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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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