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RAG2 Gene Omenn syndrome NGS Genetic Test

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RAG2 Gene Omenn syndrome NGS Genetic Test

Short Name: RAG2 Gene Omenn Syndrome Test

Also known as: RAG2 Gene Sequencing, Omenn Syndrome Genetic Test

RAG2 Gene Omenn syndrome NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood, Extracted DNA, or FTA Card samples. Results in 3-4 weeks. Free home collection in 300+ cities across India.

Next-Generation Sequencing (NGS)Pediatric🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose Omenn Syndrome by detecting mutations in the RAG2 gene using Next-Generation Sequencing (NGS) technology, guiding treatment decisions and genetic counseling.

Test Code
5076
Price
₹20,000
Sample Type
Blood, Extracted DNA, or FTA Card
Result Time
3-4 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No specific preparation required. Ensure patient identification and consent.

Method: Venipuncture or Finger prick

Step 2

Laboratory Analysis

Follow standard phlebotomy procedures. Use appropriate collection tubes.

Step 3

Report Delivery

Label samples correctly and transport to lab under ambient conditions.

Timeline: 3-4 weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor to understand the test and implications.
2
During the Test:Sample collection as per instructions.
3
After the Test:Wait for report and discuss results with healthcare provider.

About This Test

Who Should Get This Test

To diagnose Omenn Syndrome by detecting mutations in the RAG2 gene using Next-Generation Sequencing (NGS) technology, guiding treatment decisions and genetic counseling.

How to Prepare

  • No fasting required
  • Bring identification and prescription
  • Inform about any medications

Doctor's Notes

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

"Early genetic testing for Omenn Syndrome is crucial for timely intervention and management to prevent life-threatening complications."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood, Extracted DNA, or FTA Card
Sample VolumeVaries
ContainerEDTA tube or FTA Card
Collection MethodVenipuncture or Finger prick

Sample Stability

Blood: 24 hours at room temperature
DNA: Stable for longer periods
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient volume
  • Incorrect labeling

Understanding Your Results

Results indicate the presence or absence of mutations in the RAG2 gene associated with Omenn Syndrome.
📊

Mutation detected

Consistent with Omenn Syndrome, clinical correlation and genetic counseling advised.

📊

No mutation detected

Omenn Syndrome unlikely, but consider other tests if symptoms persist.

⚠️ When to Consult a Doctor:

If symptoms of Omenn Syndrome are present, or if family history suggests immunodeficiency, consult a geneticist or immunologist immediately.

Limitations

  • May not detect all types of mutations
  • Requires clinical correlation
  • Genetic counseling recommended

Risks & Considerations

  • Minor bruising at puncture site
  • Rare infection risk

Interfering Factors

  • Sample contamination
  • Degraded DNA
  • Hemolyzed sample

Compare With Similar Tests

TestRAG2 Gene Omenn syndrome NGS Genetic TestRAG1 Gene TestImmunoglobulin Levels
ComparisonRAG2 Gene Omenn syndrome NGS Genetic TestSimilar test for RAG1 gene mutations in immunodeficiency.Blood test for immune function, but not genetic.

Frequently Asked Questions

What is Omenn Syndrome?
Omenn Syndrome is a rare and severe form of combined immunodeficiency caused by mutations in the RAG2 gene, leading to immune system dysfunction.
What causes Omenn Syndrome?
It is caused by mutations in the RAG2 gene, which is crucial for the development and function of T and B lymphocytes.
What are the symptoms of Omenn Syndrome?
Symptoms include severe eczema, enlarged lymph nodes and spleen, chronic diarrhea, failure to thrive, and recurrent infections, often appearing in infancy.
How is Omenn Syndrome diagnosed?
Diagnosis involves clinical evaluation, blood tests, immunological assessments, and genetic testing such as NGS for RAG2 gene mutations.
What is the RAG2 Gene NGS Genetic Test?
It is a Next-Generation Sequencing test that analyzes the RAG2 gene for mutations to confirm Omenn Syndrome.
What is the cost of the RAG2 Gene Omenn Syndrome NGS Genetic Test in India?
The cost is approximately INR 20,000 at DNA Labs India, with home sample collection available.
How long does it take to get the test results?
Results are typically available within 3-4 weeks after sample collection.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection for online bookings across India.
What sample types are accepted for the test?
Blood, extracted DNA, or one drop of blood on an FTA card are accepted.
Do I need to fast before the test?
No, fasting is not required for this genetic test.
What should I do if the test results are positive?
Consult a geneticist or immunologist immediately for further evaluation, treatment, and genetic counseling.
Is genetic counseling available with the test?
Yes, genetic counseling is included to help understand results and implications for family planning.
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 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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