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DNA Labs India

HCN4 Gene Brugada syndrome type 8 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

HCN4 Gene Brugada syndrome type 8 NGS Genetic Test

Also known as: Brugada Syndrome Type 8 Genetic Test, HCN4 Gene Mutation Test, Brugada Syndrome NGS Test

HCN4 Gene Brugada syndrome type 8 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS (Next-Generation Sequencing) 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.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the HCN4 Gene Brugada Syndrome Type 8 NGS Genetic Test is to identify pathogenic mutations in the HCN4 gene that cause Brugada Syndrome Type 8. This aids in diagnosis, risk assessment for sudden cardiac events, family planning, and guiding personalized management strategies for affected individuals and their relatives.

Test Code
5197
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 (Next-Generation Sequencing)
Step 1

Sample Collection

No special preparation is required. Inform the healthcare provider about any medications or medical conditions. A genetic counseling session is recommended to discuss family history and test implications.

Method: Blood draw or saliva collection

Step 2

Laboratory Analysis

A trained phlebotomist will collect a blood sample via venipuncture or a saliva sample using a provided kit. The process is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding. Resume normal activities unless advised otherwise. Store the sample as per instructions if self-collected.

Timeline: 3-4 weeks

Patient Instructions

1
Before the Test:Undergo genetic counseling to discuss test purpose, implications, and family history. Provide informed consent and ensure sample collection instructions are followed.
2
During the Test:Sample collection as per standard procedures. The sample is processed in the lab using NGS technology for mutation analysis.
3
After the Test:Review results with a healthcare provider. Discuss management options, family screening, and lifestyle modifications based on findings.

About This Test

Who Should Get This Test

The purpose of the HCN4 Gene Brugada Syndrome Type 8 NGS Genetic Test is to identify pathogenic mutations in the HCN4 gene that cause Brugada Syndrome Type 8. This aids in diagnosis, risk assessment for sudden cardiac events, family planning, and guiding personalized management strategies for affected individuals and their relatives.

How to Prepare

  • Ensure proper patient identification and labeling
  • Use sterile collection equipment
  • Follow kit instructions for saliva collection
  • Transport sample to the lab within specified stability period

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Genetic testing for Brugada Syndrome is crucial for early detection and management, especially in families with a history of sudden cardiac death. It helps in risk stratification and guiding preventive measures."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Sample Stability

Blood sample stable for 48 hours at 2-8°C
Extracted DNA stable for longer periods at -20°C
FTA card samples stable at room temperature
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Incorrect labeling or documentation
  • Contaminated or degraded sample

Understanding Your Results

Results should be interpreted by a qualified geneticist or cardiologist in the context of clinical findings and family history. Genetic counseling is essential for understanding implications.
Positive Result: Pathogenic variant detected in HCN4 gene, indicating increased risk for Brugada Syndrome. Clinical correlation and family screening recommended.
Negative Result: No pathogenic variant detected. Does not completely rule out Brugada Syndrome if clinical suspicion remains high.
Variant of Uncertain Significance (VUS): Genetic change identified but clinical significance unknown. Further testing or family studies may be needed.
⚠️ When to Consult a Doctor:

Consult a cardiologist or geneticist if you experience symptoms like fainting, palpitations, or chest pain, or if you have a family history of Brugada Syndrome or sudden cardiac death. Seek immediate medical attention for severe symptoms.

Limitations

  • May not detect all genetic variants or mutations
  • Results require interpretation by a qualified geneticist or cardiologist
  • Cannot predict disease severity or onset with certainty
  • Variants of uncertain significance may necessitate further testing

Risks & Considerations

  • Minimal risk from blood draw, such as bruising or infection
  • Psychological impact of results, including anxiety or stress
  • Potential for incidental findings or variants of uncertain significance

Interfering Factors

  • Sample contamination or degradation
  • Technical errors in sequencing or analysis
  • Presence of variants of uncertain significance
  • Inadequate sample volume or quality

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Frequently Asked Questions

What is the HCN4 Gene Brugada Syndrome Type 8 NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the HCN4 gene associated with Brugada Syndrome Type 8, a rare heart rhythm disorder.
Who should consider this test?
Individuals with a family history of Brugada Syndrome, unexplained fainting, palpitations, abnormal ECG findings, or symptoms like chest pain and irregular heartbeats.
How is the test performed?
A blood or saliva sample is collected and analyzed using NGS technology to identify mutations in the HCN4 gene.
What is the cost of the test?
The test costs INR 20000.0, with home sample collection available across India at no additional charge.
How long does it take to get results?
Results are typically available within 3-4 weeks after sample collection.
Is fasting required for this test?
No, fasting is not required for this genetic test.
What do the results mean?
Results indicate whether a pathogenic mutation in the HCN4 gene is detected. Positive results suggest increased risk for Brugada Syndrome, while negative results may not rule out the condition entirely.
Is genetic counseling provided?
Yes, DNA Labs India offers genetic counseling to help interpret results and discuss implications for family planning and management.
Can this test be done at home?
Yes, DNA Labs India provides free home sample collection for online bookings across many cities in India.
What are the risks of the test?
Risks are minimal, such as bruising from blood draw. Psychological impact of results is possible, so counseling is recommended.
How accurate is the test?
The test uses advanced NGS technology for high accuracy, but no genetic test can detect all mutations. Results should be correlated with clinical findings.
What should I do after receiving results?
Consult a cardiologist or geneticist to discuss results, management options, and family screening. Follow recommended lifestyle and medical interventions.
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.

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