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.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
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
Sample Collection
No specific preparation required. Provide clinical history and family pedigree during genetic counseling.
Method: Venipuncture or FTA Card
Laboratory Analysis
Blood sample collected via venipuncture or one drop on FTA card by trained phlebotomist.
Report Delivery
Sample sent to lab for analysis. Genetic counseling session recommended to discuss results.
Timeline: 3 to 4 Weeks
Patient Instructions
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 Dr Pasupathy Arumugam — 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 Stability
- Hemolyzed samples
- Insufficient sample volume
- Incorrect labeling
Understanding Your Results
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.
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?
What is Sudden Infant Death Syndrome (SIDS)?
How does SCN5A mutation relate to SIDS?
Who should consider this genetic test?
How is the test performed?
What sample is required for the test?
How long does it take to get results?
What does a positive result mean?
What does a negative result mean?
Is genetic counseling provided?
What is the cost of the test?
Is the test covered by insurance?
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₹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.
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✓ 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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