MAGT1 Gene Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia NGS Genetic Test
MAGT1 Gene Immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia 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 3-4 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 mutations in the MAGT1 gene for the diagnosis of X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia.
- Test Code
- 2602
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3-4 weeks
- Fasting Required
- No
- Method
- NGS Technology
Sample Collection
Genetic counseling session recommended to discuss family history and draw a pedigree chart.
Method: Venipuncture
Laboratory Analysis
Your sample is analyzed using NGS Technology in our laboratory.
Report Delivery
A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.
Timeline: 3-4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the MAGT1 gene for the diagnosis of X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia.
How to Prepare
- Blood sample collection via venipuncture or use of FTA card for one drop of blood.
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"This NGS test is essential for accurate diagnosis and management of MAGT1-related immunodeficiency, helping to prevent severe infections and cancer."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of MAGT1 gene immunodeficiency. Genetic counseling and management recommended.
No pathogenic variant detected
MAGT1 gene mutation not identified. Clinical correlation advised.
If symptoms such as recurrent infections, chronic diarrhea, or growth delay are present, or if there is a family history of X-linked immunodeficiency.
Risks & Considerations
- ●Minimal risk associated with blood draw
- ●Potential psychological impact of genetic results
Frequently Asked Questions
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