Epilepsy Panel NGS Genetic Test
Short Name: Epilepsy NGS Panel
Also known as: Epilepsy Genetic NGS Panel, Seizure Disorder Panel, Epilepsy Mutation Analysis
Epilepsy Panel 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 the date of sample receipt at the laboratory.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The primary purpose of the Epilepsy Panel NGS Genetic Test is to detect pathogenic variants in genes linked to epilepsy, thereby aiding clinicians in establishing a molecular diagnosis, differentiating epilepsy subtypes, guiding treatment decisions, and providing information about recurrence risks for family planning.
- Test Code
- 3856
- ICD Code
- G40.9
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 weeks from the date of sample receipt at the laboratory.
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No special preparation or fasting is required. However, a clinical history and genetic counseling session are recommended before the test to establish a detailed pedigree and ensure appropriate test selection.
Method: Venipuncture / Finger-prick
Laboratory Analysis
A single blood sample (3-5 mL) is collected from a vein, or a dried blood spot may be obtained using a finger-prick. The procedure is quick and requires minimal discomfort.
Report Delivery
The sample is labeled and transported to the laboratory. No specific aftercare is necessary. Patients can resume normal activities immediately.
Timeline: 3 to 4 weeks from the date of sample receipt at the laboratory.
Patient Instructions
About This Test
Who Should Get This Test
The primary purpose of the Epilepsy Panel NGS Genetic Test is to detect pathogenic variants in genes linked to epilepsy, thereby aiding clinicians in establishing a molecular diagnosis, differentiating epilepsy subtypes, guiding treatment decisions, and providing information about recurrence risks for family planning.
How to Prepare
- No special preparation needed.
- Please provide a valid prescription or doctor's referral.
- A genetic counseling session will be scheduled to draw a pedigree chart.
- Sample collection can be done at home or at a nearby lab.
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This panel is particularly useful in early-onset epilepsy and cases where a specific genetic syndrome is suspected. Combining genetic results with clinical EEG and imaging improves diagnostic accuracy and may help in selecting first-line therapies."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Clotted or hemolyzed sample
- Improper labeling
- Insufficient sample quantity
- Sample received in improper container (e.g., heparin tube)
- Missing clinical history or consent form
Understanding Your Results
No pathogenic variants detected
A genetic cause was not identified in the analyzed panel. This does not rule out a genetic etiology, and additional testing may be considered.
Pathogenic or likely pathogenic variant identified
A definitive cause is identified. This information can be used for clinical management, prognosis, and recurrence risk counseling.
Variant of uncertain significance (VUS)
A genetic variant was found, but its role in disease is unclear. Review of family studies may reclassify the variant in the future.
You should consult your neurologist or genetic counselor to determine if the Epilepsy Panel NGS Genetic Test is appropriate for you, and to discuss the results of the test in depth.
Limitations
- ⚠NGS panel does not detect all types of genetic variants, including large structural rearrangements, deep intronic variants, or repeat expansions.
- ⚠A negative result does not exclude a genetic cause, as undetected variants or unknown genes may be responsible.
- ⚠Variants of uncertain significance (VUS) may be reported, requiring additional family studies for interpretation.
- ⚠The test is not intended for all cases of epilepsy; clinical evaluation is essential.
- ⚠Genetic counseling is recommended to understand limitations and implications.
Risks & Considerations
- ●Minimal risk of pain or bruising at the venipuncture site
- ●Infection (very rare)
- ●Psychological impact from unexpected or uncertain genetic findings
Interfering Factors
- ●Insufficient DNA quality or quantity
- ●Contamination during sample collection
- ●Low sequencing depth in specific gene regions (e.g., GC-rich regions)
- ●Presence of large deletions/duplications not detected by NGS alone
- ●Mosaic variants may be below detection threshold
Compare With Similar Tests
| Test | Epilepsy Panel NGS Genetic Test | ||
|---|---|---|---|
| Comparison | Epilepsy Panel NGS Genetic Test |
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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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