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DNA Labs India

SCN1B Gene Brugada syndrome type 5 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

SCN1B Gene Brugada syndrome type 5 NGS Genetic Test

Also known as: SCN1B gene test, Brugada syndrome type 5 genetic test, SCN1B mutation analysis

SCN1B Gene Brugada syndrome type 5 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses 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

To detect mutations in the SCN1B gene associated with Brugada syndrome type 5, enabling accurate diagnosis, risk assessment, and personalized management of cardiac arrhythmias.

Test Code
5194
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
Step 1

Sample Collection

No specific preparation required. Provide clinical history and family pedigree during genetic counseling.

Method: Blood draw

Step 2

Laboratory Analysis

Blood sample will be drawn by a trained phlebotomist. For FTA card, a drop of blood is applied.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Resume normal activities.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Undergo genetic counseling to understand implications. Provide detailed family medical history.
2
During the Test:Sample collection takes a few minutes. No discomfort beyond a blood draw.
3
After the Test:Wait for results. Genetic counselor will explain findings and next steps.

About This Test

Who Should Get This Test

To detect mutations in the SCN1B gene associated with Brugada syndrome type 5, enabling accurate diagnosis, risk assessment, and personalized management of cardiac arrhythmias.

How to Prepare

  • Ensure proper identification of the patient
  • Use sterile equipment for blood collection
  • Label samples correctly with patient details
  • Transport samples at room temperature unless specified

Doctor's Notes

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

"Genetic testing for SCN1B mutations is essential for accurate diagnosis and personalized management of Brugada syndrome type 5, helping 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 MethodBlood draw

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 samples
  • Insufficient sample volume
  • Improperly labeled or contaminated samples

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the SCN1B gene. Positive results confirm genetic predisposition to Brugada syndrome type 5, while negative results may require further clinical evaluation.
📊

Positive for pathogenic variant

Confirms diagnosis of Brugada syndrome type 5. Risk of arrhythmias increased. Consult cardiologist for management.

📊

Negative for pathogenic variant

No SCN1B mutations detected. Symptoms may be due to other causes. Clinical correlation recommended.

📊

Variant of uncertain significance

Genetic change identified but clinical significance unknown. Further testing and family studies may be needed.

⚠️ When to Consult a Doctor:

Consult a cardiologist or genetic specialist if you experience symptoms like fainting, palpitations, or have a family history of sudden cardiac death, regardless of test results.

Limitations

  • May not detect all possible mutations in the SCN1B gene
  • Variants of uncertain significance may be identified
  • Does not rule out other genetic causes of Brugada syndrome

Risks & Considerations

  • Minimal risks from blood draw, such as bruising or infection
  • Psychological impact of genetic results
  • Potential for uncertain results requiring further testing

Interfering Factors

  • Sample contamination
  • Degraded DNA quality
  • Hemolyzed blood samples

Compare With Similar Tests

TestSCN1B Gene Brugada syndrome type 5 NGS Genetic TestECG TestStress TestSCN5A Gene Test
ComparisonSCN1B Gene Brugada syndrome type 5 NGS Genetic TestECG detects electrical abnormalities but cannot identify genetic mutations. Genetic test provides definitive diagnosis.Stress test evaluates heart response to exercise. Genetic test identifies underlying genetic cause.SCN5A test for other Brugada syndrome types. SCN1B test specifically for type 5.

Frequently Asked Questions

What is SCN1B Gene Brugada Syndrome Type 5?
It is a genetic disorder caused by mutations in the SCN1B gene, leading to abnormal heart rhythms and risk of sudden cardiac arrest.
How is the SCN1B Gene Brugada Syndrome Type 5 NGS Genetic Test performed?
The test uses Next-Generation Sequencing (NGS) to analyze DNA from a blood sample for mutations in the SCN1B gene.
What are the symptoms of Brugada syndrome type 5?
Symptoms include fainting, dizziness, rapid heartbeat, shortness of breath, and chest pain, often triggered by stress or activity.
Who should consider getting this genetic test?
Individuals with family history of Brugada syndrome, unexplained cardiac symptoms, or abnormal ECG findings should consider testing.
What is the cost of the SCN1B Gene Brugada Syndrome Type 5 NGS Genetic Test in India?
The test costs INR 20,000 at DNA Labs India, with free home sample collection available.
How long does it take to receive the test results?
Results are typically available within 3 to 4 weeks after sample collection.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection across many cities in India.
What do the test results mean?
Positive results indicate a genetic mutation linked to Brugada syndrome type 5. Negative results suggest no mutation detected, but clinical evaluation may be needed.
Are there any risks associated with the genetic test?
Risks are minimal, mainly from blood draw, such as bruising. Psychological impact of results is possible.
How accurate is the SCN1B Gene Brugada Syndrome Type 5 NGS Genetic Test?
The test is highly accurate using NGS technology, but may not detect all mutations or variants of uncertain significance.
Can this test be used for prenatal diagnosis?
Prenatal testing may be possible but requires consultation with a genetic specialist for appropriate counseling and procedures.
What should I do after receiving the test results?
Consult a cardiologist or genetic counselor to understand the results, discuss management options, and consider family screening.
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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