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SCN1A Gene Early infantile epileptic encephalopathy type 6 NGS Genetic Test

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SCN1A Gene Early infantile epileptic encephalopathy type 6 NGS Genetic Test

Short Name: SCN1A EIEE6 NGS Test

Also known as: SCN1A Gene Sequencing, EIEE6 Genetic Test, SCN1A Next-Generation Sequencing Test

SCN1A Gene Early infantile epileptic encephalopathy type 6 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 weeks from sample receipt. Additional time may be needed if parental or confirmatory studies are required.. Free home collection in 300+ cities across India.

NGS Genetic TestInfants and Children🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

The purpose of this NGS genetic test is to identify disease-causing variants in the SCN1A gene and provide molecular confirmation for early infantile epileptic encephalopathy type 6, enabling accurate genetic counselling, recurrence-risk assessment, and treatment guidance.

Test Code
4045
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 weeks from sample receipt. Additional time may be needed if parental or confirmatory studies are required.
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No fasting is required. Please carry the test requisition form, relevant medical records, and a valid ID. A genetic counselling session may be recommended to document family history and draw a pedigree chart.

Method: Peripheral blood draw, extracted DNA, or FTA card spot

Step 2

Laboratory Analysis

A simple blood sample is collected from a vein in the arm, or a few drops of blood are placed on an FTA card depending on the chosen option. The collection procedure is quick and minimally invasive.

Step 3

Report Delivery

You may resume normal activities immediately. The sample is transported to the laboratory at ambient temperature. The clinical report, along with raw data files, will be shared within 3 to 4 weeks.

Timeline: 3 to 4 weeks from sample receipt. Additional time may be needed if parental or confirmatory studies are required.

Patient Instructions

1
Before the Test:No fasting required. A genetic counselling session is recommended to review family history and pre-test expectations.
2
During the Test:The sample collection procedure is simple and involves either blood collection or an FTA card spot. No special precautions are needed during the procedure.
3
After the Test:After the test, the clinician will explain the result and its implications for diagnosis, treatment, and family planning.

About This Test

Who Should Get This Test

The purpose of this NGS genetic test is to identify disease-causing variants in the SCN1A gene and provide molecular confirmation for early infantile epileptic encephalopathy type 6, enabling accurate genetic counselling, recurrence-risk assessment, and treatment guidance.

How to Prepare

  • Use an EDTA tube for whole blood collection if applicable.
  • If using FTA card, let the blood spot air dry completely before packing.
  • Write the patient name and unique identifier clearly on the tube or card.
  • Transport the sample to DNA Labs India as soon as possible at ambient temperature.

Doctor's Notes

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

"A confirmed molecular diagnosis of EIEE6 is important because seizure management can be different in SCN1A-related epilepsies. Genetic testing should always be combined with detailed clinical evaluation and genetic counselling."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample VolumeAs required for DNA extraction
ContainerEDTA Tube / FTA Card
Collection MethodPeripheral blood draw, extracted DNA, or FTA card spot

Sample Stability

Whole blood in EDTA: transport at 2-8°C or ambient temperature within 24-48 hours.
Extracted DNA: store frozen until shipment.
FTA card: stable at room temperature for several weeks.
Sample Rejection Criteria:
  • Unlabelled or incorrectly labelled sample
  • Sample received in a leaking container
  • Haemolysed or clotted blood unsuitable for DNA extraction
  • Mismatched patient identifiers

Understanding Your Results

Results are interpreted by a clinical geneticist in the context of clinical presentation and family history.
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⚠️ When to Consult a Doctor:

Consult a child neurologist or clinical geneticist if an infant has recurrent seizures in the first months of life, global developmental delay, or a family history of EIEE6 or SCN1A-related epilepsy.

Risks & Considerations

  • ●Minimal risk of discomfort or bruising at the blood collection site
  • ●Rare possibility of vasovagal reaction during blood draw
  • ●Psychological impact associated with genetic results and family implications

Interfering Factors

  • ●Poor DNA quality or quantity from degraded samples
  • ●Maternal cell contamination
  • ●Contaminated or haemolysed blood sample
  • ●Incorrect sample labelling

Compare With Similar Tests

TestSCN1A Gene Early infantile epileptic encephalopathy type 6 NGS Genetic Test
ComparisonSCN1A Gene Early infantile epileptic encephalopathy type 6 NGS Genetic Test

Frequently Asked Questions

What is the cost of the SCN1A EIEE6 NGS genetic test?
The test cost is INR 20,000 at DNA Labs India. The price includes home sample collection in eligible cities and delivery of raw data files with the clinical report.
What is this test used for?
This NGS-based genetic test is used to detect pathogenic variants in the SCN1A gene that are associated with Early Infantile Epileptic Encephalopathy Type 6 (EIEE6), helping confirm the diagnosis in infants with seizures and developmental delay.
How is the sample collected?
The sample can be collected as blood in an EDTA tube, extracted DNA, or one drop of blood on an FTA card. A trained phlebotomist can also visit your home for collection in select cities.
Do I need to fast before the test?
No, fasting is not required for this genetic test. You can schedule the sample collection at your convenience.
When will I get the report?
Reports are usually available in 3 to 4 weeks after the sample reaches the laboratory and all quality checks are completed.
What is the role of NGS in this test?
NGS, or next-generation sequencing, allows comprehensive sequencing of multiple genes in a single run. For EIEE6, it focuses on SCN1A and can identify mutations that may cause the condition, even in complex cases.
What does a negative result mean?
A negative result means no pathogenic or likely pathogenic variant in the SCN1A gene was detected in the analysed sample. However, it does not rule out all genetic causes of epilepsy, and additional testing may be needed.
What does a positive result mean?
A positive result means a disease-causing variant was found in the SCN1A gene. It supports a diagnosis of EIEE6 or SCN1A-related epilepsy and helps guide treatment, prognosis, and family counselling.
Should parents also be tested?
If a pathogenic variant is identified in the child, parental testing is often recommended to determine whether the variant was inherited or arose de novo. This can be discussed during the genetic counselling session.
What are the symptoms of SCN1A EIEE6?
Symptoms usually begin in the first few months of life and include frequent seizures, developmental delay, intellectual disability, movement and coordination difficulty, abnormal muscle tone, and behavioural problems.
How can I book this test at DNA Labs India?
You can book online through the DNA Labs India website. Home sample collection is free for online bookings, and the service is available in many cities across India.
Will I receive raw data and reports?
Yes, DNA Labs India provides transparent reporting. Along with the clinical report, you receive raw data files, FASTQ, and VCF files for the SCN1A EIEE6 NGS genetic test.
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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For Hospitals & Clinics

Reference 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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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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