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GRIN2A Gene Epilepsy with neurodevelopmental defects NGS Genetic Test

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GRIN2A Gene Epilepsy with neurodevelopmental defects NGS Genetic Test

Short Name: GRIN2A NGS Test

Also known as: GRIN2A-related epilepsy genetic test, GRIN2A gene sequencing test, Epilepsy neurodevelopmental defects NGS panel

GRIN2A Gene Epilepsy with neurodevelopmental defects 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 after sample submission. Occasional delays may occur due to repeat testing or technical issues.. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to detect mutations in the GRIN2A gene that are associated with epilepsy and neurodevelopmental defects. Early genetic diagnosis helps in personalized treatment planning, prognostication, and genetic counseling for affected families.

Test Code
4062
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 weeks after sample submission. Occasional delays may occur due to repeat testing or technical issues.
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No special preparation is required. However, a clinical history and genetic counseling session is recommended. Please bring any prior medical reports or imaging records.

Method: Peripheral blood draw or FTA card blood spot

Step 2

Laboratory Analysis

A blood sample is drawn by a trained phlebotomist in an EDTA tube. Alternatively, a few drops of blood can be applied on an FTA card for convenience.

Step 3

Report Delivery

There are no restrictions after sample collection. The sample is transported to the laboratory at ambient temperature. You may return to your normal activities.

Timeline: 3 to 4 weeks after sample submission. Occasional delays may occur due to repeat testing or technical issues.

Patient Instructions

1
Before the Test:No fasting needed. Genetic counseling is advised before the test to discuss risks, benefits, and expected outcomes.
2
During the Test:You may experience mild discomfort during blood collection. The entire procedure takes about 5-10 minutes.
3
After the Test:Results will be available in 3 to 4 weeks. You will be notified when the report is ready.

About This Test

Who Should Get This Test

The purpose of this test is to detect mutations in the GRIN2A gene that are associated with epilepsy and neurodevelopmental defects. Early genetic diagnosis helps in personalized treatment planning, prognostication, and genetic counseling for affected families.

How to Prepare

  • Collect 2-3 ml blood in an EDTA vacutainer
  • For FTA card, apply one drop of blood on each marked circle and allow to air dry
  • Label the sample with patient's full name, date of birth, and collection date

Doctor's Notes

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

"A detailed family history and genetic counseling are essential for accurate interpretation of GRIN2A gene variants and reproductive risk assessment."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume2-3 ml Blood or 1-2 µg DNA
ContainerEDTA tube or FTA card
Collection MethodPeripheral blood draw or FTA card blood spot

Sample Stability

Blood (EDTA): 72 hours at room temperature
Extracted DNA: 1 week at 2-8°C
FTA card: 1 year at room temperature
Sample Rejection Criteria:
  • Clotted or hemolyzed blood sample
  • Improperly labeled sample
  • Sample received more than 5 days after collection

Understanding Your Results

The test result is interpreted by a clinical geneticist. Findings should be evaluated in the context of the patient's clinical presentation, family history, and other laboratory investigations.
📊

Pathogenic variant identified

The variant is associated with GRIN2A-related epilepsy. Genetic counseling and familial testing are recommended.

📊

Variant of uncertain significance (VUS)

Further studies may be needed to clarify the clinical significance. Consider segregation analysis in family members.

📊

No pathogenic variant detected

No clinically significant mutation found in the GRIN2A gene. A broader epilepsy gene panel may be considered.

⚠️ When to Consult a Doctor:

If you receive a positive result or a VUS, it is recommended to consult a neurologist and a clinical geneticist for further management, treatment planning, and family counseling.

Limitations

  • NGS may not detect large gene rearrangements, repeat expansions, or deep intronic variants
  • Negative results do not rule out a genetic cause of epilepsy
  • Variants of uncertain significance may require additional familial testing

Risks & Considerations

  • Slight pain or bruising at the blood draw site
  • Rare risk of infection at needle site
  • Psychological impact of results

Interfering Factors

  • Bone marrow transplant from another person may alter DNA test results
  • Recent blood transfusion can affect DNA extraction and analysis
  • Sample contamination with microbial DNA

Compare With Similar Tests

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Frequently Asked Questions

What is the GRIN2A gene epilepsy with neurodevelopmental defects NGS genetic test?
It is a next-generation sequencing test that analyses the coding regions of the GRIN2A gene to identify mutations associated with early-onset epilepsy and neurodevelopmental defects.
How is this test performed?
A blood sample is collected from the patient. DNA is extracted and enriched for the GRIN2A gene, then sequenced on an NGS platform. Bioinformatics analysis identifies variants.
Do I need to fast before the test?
No, fasting is not required for this genetic test. You can continue your routine diet and medications unless advised otherwise.
What is the sample type?
The sample can be 2-3 ml peripheral blood in an EDTA tube, extracted DNA, or a few drops of blood on an FTA card.
How long will the results take?
The reports are issued within 3 to 4 weeks after the sample reaches the laboratory.
What does a positive result mean?
A pathogenic mutation in the GRIN2A gene confirms the genetic cause of epilepsy and can help guide treatment and prognosis.
Can this test be done for children?
Yes, this test is suitable for children and newborns with seizures or developmental delay, as early diagnosis can improve management.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test in over 200 cities across India.
What is the cost of the GRIN2A NGS test?
The test costs Rs 20000.0 at DNA Labs India, which is inclusive of all charges.
Is genetic counseling included with the test?
Yes, a genetic counseling session is part of the pre-test process to draw a pedigree and discuss the implications of testing.
Will I receive raw data files?
Yes, DNA Labs India provides raw data, FASTQ, and VCF files along with the clinical report upon request.
Can a negative result rule out epilepsy?
No. A negative result means no clinically significant mutation was found in the GRIN2A gene. It does not rule out other genetic or non-genetic causes.
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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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 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.

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