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DNM2 Gene Centronuclear Myopathy Type 1 NGS Genetic Test

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DNM2 Gene Centronuclear Myopathy Type 1 NGS Genetic Test

Short Name: DNM2 CNM Type 1 NGS Test

Also known as: Autosomal Dominant Centronuclear Myopathy, CNM Type 1

DNM2 Gene Centronuclear Myopathy Type 1 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood, Extracted DNA, or FTA Card sample samples. Results in 3 to 4 weeks. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To identify mutations in the DNM2 gene that cause Centronuclear Myopathy Type 1, aiding in diagnosis and management.

Test Code
1538
Price
₹20,000
Sample Type
Blood, Extracted DNA, or FTA Card sample
Result Time
3 to 4 weeks
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

No special preparation required. Ensure proper identification and informed consent.

Method: Venipuncture or Saliva collection

Step 2

Laboratory Analysis

Sample collected via venipuncture or saliva method with minimal discomfort.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Keep sample at ambient room temperature.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Consult with a genetic counselor for family history assessment and informed consent.
2
During the Test:Sample collection is quick, safe, and performed by trained professionals.
3
After the Test:Results will be available in 3-4 weeks. Follow up with your physician for interpretation and management.

About This Test

Who Should Get This Test

To identify mutations in the DNM2 gene that cause Centronuclear Myopathy Type 1, aiding in diagnosis and management.

How to Prepare

  • Use sterile collection equipment
  • Label samples correctly with patient details
  • Transport samples at room temperature

Doctor's Notes

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

"Genetic testing for DNM2 mutations can confirm diagnosis and aid in genetic counseling for families affected by centronuclear myopathy."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood, Extracted DNA, or FTA Card sample
Collection MethodVenipuncture or Saliva collection

Sample Stability

Room temperature7 days
Sample Rejection Criteria:
  • Insufficient sample volume
  • Sample contaminated
  • Improper storage or handling

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the DNM2 gene. A positive result confirms the diagnosis of Centronuclear Myopathy Type 1.
📊

Positive

Pathogenic mutation detected; confirms diagnosis and supports genetic counseling

📊

Negative

No pathogenic mutation detected; clinical correlation needed to rule out other causes

⚠️ When to Consult a Doctor:

If symptoms of muscle weakness or wasting are present, or if there is a family history of centronuclear myopathy.

Limitations

  • May not detect all types of mutations
  • Results require clinical correlation
  • Not a substitute for comprehensive clinical evaluation

Risks & Considerations

  • Minor bruising at blood draw site
  • Very low risk of infection

Interfering Factors

  • Poor sample quality
  • Contamination of DNA sample
  • Hemolyzed blood sample

Compare With Similar Tests

TestDNM2 Gene Centronuclear Myopathy Type 1 NGS Genetic TestMTM1 Gene Centronuclear Myopathy Test
ComparisonDNM2 Gene Centronuclear Myopathy Type 1 NGS Genetic Test

Frequently Asked Questions

What is the DNM2 Gene Centronuclear Myopathy Type 1 NGS Genetic Test?
It is a genetic test that uses next-generation sequencing to detect mutations in the DNM2 gene, which causes centronuclear myopathy type 1.
Who should take this test?
Individuals with symptoms like muscle weakness, wasting, or a family history of centronuclear myopathy should consider this test.
What are the symptoms of DNM2-related centronuclear myopathy?
Common symptoms include muscle weakness, difficulty walking, respiratory problems, and scoliosis.
How is the test performed?
A blood or saliva sample is collected and analyzed using NGS technology to identify DNM2 gene mutations.
What is the cost of the test?
The test costs INR 20000, which includes sample collection, analysis, and result interpretation.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection across many cities in India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks after sample collection.
What does a positive result mean?
A positive result confirms the presence of a pathogenic DNM2 mutation, supporting a diagnosis of centronuclear myopathy type 1.
Can this test be used for prenatal diagnosis?
This test is primarily for diagnostic purposes; consult a genetic counselor for prenatal testing options.
Are there any risks involved?
Risks are minimal, such as minor bruising from blood draw or very low infection risk.
How accurate is the NGS technology?
NGS is highly accurate for detecting mutations, but results should be correlated with clinical findings.
Where can I get this test done?
This test is available through DNA Labs India with home collection or walk-in options at various locations.
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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LIMS Integration

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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