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DNA Labs India

SCN5A Gene Sudden infant death syndrome, susceptibility to NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

SCN5A Gene Sudden infant death syndrome, susceptibility to NGS Genetic Test

Short Name: SCN5A Gene SIDS NGS Genetic Test

Also known as: SCN5A Mutation Test for SIDS, SIDS Genetic Susceptibility Test, SCN5A Gene Sequencing for SIDS

SCN5A Gene Sudden infant death syndrome, susceptibility to NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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.

Genetic TestInfants🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify genetic mutations in the SCN5A gene that may increase susceptibility to sudden infant death syndrome (SIDS), enabling risk assessment and informed decision-making for families.

Test Code
5291
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 Technology
Step 1

Sample Collection

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

Method: Venipuncture or FTA Card

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or one drop on FTA card by trained phlebotomist.

Step 3

Report Delivery

Sample sent to lab for analysis. Genetic counseling session recommended to discuss results.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling session to discuss test implications and draw family pedigree.
2
During the Test:Sample collection procedure as per standard protocols.
3
After the Test:Wait for report delivery in 3-4 weeks. Schedule follow-up counseling to discuss results.

About This Test

Who Should Get This Test

To identify genetic mutations in the SCN5A gene that may increase susceptibility to sudden infant death syndrome (SIDS), enabling risk assessment and informed decision-making for families.

How to Prepare

  • Ensure proper identification of patient
  • Use sterile collection equipment
  • Label samples correctly
  • Transport samples at recommended temperature

Doctor's Notes

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

"Genetic testing for SCN5A mutations can help assess susceptibility to SIDS and guide preventive measures for at-risk families."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Sample Stability

Blood: 2-8°C for 72 hours
FTA Card: Room temperature for extended periods
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient sample volume
  • Incorrect labeling

Understanding Your Results

Results indicate the presence or absence of SCN5A gene mutations associated with SIDS susceptibility. Consult a genetic counselor for detailed interpretation.
📊

Negative

No pathogenic variants detected in SCN5A gene. Reduced genetic risk, but other factors may contribute.

📊

Positive

Pathogenic variant detected. Increased genetic susceptibility to SIDS. Recommend genetic counseling and cardiac monitoring.

📊

VUS

Variant of uncertain significance. Further testing and family studies may be needed.

⚠️ When to Consult a Doctor:

Consult a healthcare provider or genetic counselor if results are positive or if there is a family history of SIDS or cardiac conditions.

Limitations

  • Test may not detect all genetic variants
  • Results require interpretation by a genetic counselor
  • Does not diagnose SIDS definitively, only assesses genetic susceptibility

Risks & Considerations

  • Minimal risk from blood draw, such as bruising or infection
  • Psychological impact of genetic results

Interfering Factors

  • Poor sample quality
  • Contaminated DNA
  • Technical errors in sequencing

Frequently Asked Questions

What is the SCN5A gene?
The SCN5A gene encodes a sodium channel protein essential for regulating heart electrical activity. Mutations can lead to arrhythmias.
What is Sudden Infant Death Syndrome (SIDS)?
SIDS is the unexplained death of an otherwise healthy infant, usually during sleep, often without warning signs.
How does SCN5A mutation relate to SIDS?
Mutations in SCN5A can disrupt heart rhythm, potentially causing fatal arrhythmias that may contribute to SIDS.
Who should consider this genetic test?
Families with a history of SIDS, unexplained infant deaths, or known SCN5A mutations should consider testing.
How is the test performed?
The test uses next-generation sequencing (NGS) to analyze the SCN5A gene from a blood or DNA sample.
What sample is required for the test?
Blood, extracted DNA, or one drop of blood on an FTA card can be used.
How long does it take to get results?
Results are typically available in 3 to 4 weeks after sample collection.
What does a positive result mean?
A positive result indicates a pathogenic SCN5A variant, suggesting increased genetic susceptibility to SIDS. Genetic counseling is recommended.
What does a negative result mean?
A negative result means no pathogenic variants were detected, reducing genetic risk, but other factors may still contribute.
Is genetic counseling provided?
Yes, DNA Labs India offers genetic counseling sessions to discuss test results and implications.
What is the cost of the test?
The test costs INR 20000, with free home sample collection available across India.
Is the test covered by insurance?
Coverage varies by insurance plan. Check with your provider for details on genetic testing coverage.
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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