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.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
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
Sample Collection
No specific preparation required. Provide clinical history and family pedigree during genetic counseling.
Method: Blood draw
Laboratory Analysis
Blood sample will be drawn by a trained phlebotomist. For FTA card, a drop of blood is applied.
Report Delivery
Apply pressure to the puncture site to prevent bleeding. Resume normal activities.
Timeline: 3 to 4 Weeks
Patient Instructions
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 Dr SULOCHANA HEMCHANDRA HOLLA — 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 Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Improperly labeled or contaminated samples
Understanding Your Results
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.
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
| Test | SCN1B Gene Brugada syndrome type 5 NGS Genetic Test | ECG Test | Stress Test | SCN5A Gene Test |
|---|---|---|---|---|
| Comparison | SCN1B Gene Brugada syndrome type 5 NGS Genetic Test | ECG 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?
How is the SCN1B Gene Brugada Syndrome Type 5 NGS Genetic Test performed?
What are the symptoms of Brugada syndrome type 5?
Who should consider getting this genetic test?
What is the cost of the SCN1B Gene Brugada Syndrome Type 5 NGS Genetic Test in India?
How long does it take to receive the test results?
Is home sample collection available for this test?
What do the test results mean?
Are there any risks associated with the genetic test?
How accurate is the SCN1B Gene Brugada Syndrome Type 5 NGS Genetic Test?
Can this test be used for prenatal diagnosis?
What should I do after receiving the test results?
Related Tests
APOB Gene Hypercholesterolemia type B autosomanl dominant NGS Genetic Test
₹20,000MICM (Maternally Inherited Cardiomyopathy) Mutation Detection Test
₹10,500EPHX2 Gene Hypercholesterolemia, familial, due to LDLR defect, modifier of NGS Genetic Test
₹20,000DSC2 Gene Arrhythmogenic right ventricular cardiomyopathy type 11 NGS Genetic Test
₹20,000KCNA5 Gene Atrial fibrillation type 7 NGS Genetic Test
₹20,000MYH6 Gene Atrial septal defect type 3 NGS Genetic Test
₹20,000Reference 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.
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.
