NF2 Gene Neurofibromatosis type 2 NGS Genetic Test
Short Name: NF2 NGS Genetic Test
Also known as: NF2 genetic test, Merlin gene test, Neurofibromatosis type 2 DNA test
NF2 Gene Neurofibromatosis type 2 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. 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
To detect mutations in the NF2 gene for diagnosis of Neurofibromatosis type 2, aiding in clinical management and genetic counseling.
- Test Code
- 2914
- 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
- Next-Generation Sequencing (NGS)
Sample Collection
Provide clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of family members affected with NF2.
Method: Venipuncture
Laboratory Analysis
Standard blood draw procedure; for FTA card, a drop of blood is applied.
Report Delivery
Apply pressure to the puncture site; store sample at ambient room temperature.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To detect mutations in the NF2 gene for diagnosis of Neurofibromatosis type 2, aiding in clinical management and genetic counseling.
How to Prepare
- Ensure proper identification of the patient
- Use sterile equipment for blood collection
- Label samples correctly with patient details
- Transport samples to the lab within specified stability period
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"NF2 is a rare genetic disorder requiring early diagnosis for management. Genetic testing via NGS is crucial for accurate identification and family counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted blood sample
- Insufficient sample volume
- Incorrect labeling or missing patient information
Understanding Your Results
Positive for NF2 mutation
Confirms diagnosis of Neurofibromatosis type 2; genetic counseling and management recommended.
Negative for NF2 mutation
No pathogenic variant detected; clinical correlation and additional testing may be needed if symptoms persist.
Variant of uncertain significance
Further analysis and family studies recommended for clarification.
Consult a doctor if you experience symptoms like hearing loss, balance issues, or vision problems, especially with a family history of NF2. After testing, discuss results with a genetic counselor or neurologist for appropriate management.
Limitations
- ⚠May not detect all types of mutations, such as large deletions
- ⚠Requires genetic counseling for interpretation
- ⚠Results should be correlated with clinical findings
Risks & Considerations
- ●Minimal risk from blood draw, such as bruising or infection
- ●Psychological impact of genetic results; counseling advised
Interfering Factors
- ●Contaminated or degraded DNA sample
- ●Incorrect sample collection or storage
- ●Recent blood transfusion may affect results
Compare With Similar Tests
| Test | NF2 Gene Neurofibromatosis type 2 NGS Genetic Test | MRI Scan | Hearing Test | Sanger Sequencing | NF1 Genetic Test |
|---|---|---|---|---|---|
| Comparison | NF2 Gene Neurofibromatosis type 2 NGS Genetic Test |
Frequently Asked Questions
What is Neurofibromatosis type 2 (NF2)?
What are the common symptoms of NF2?
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What is the NF2 NGS Genetic Test?
What is the cost of the NF2 NGS Genetic Test in India?
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