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SAMD9 Gene Mirage syndrome NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

SAMD9 Gene Mirage syndrome NGS Genetic Test

Short Name: SAMD9 NGS Test

Also known as: SAMD9 Syndrome, Mirage Syndrome

SAMD9 Gene Mirage syndrome 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 to 4 Weeks. Free home collection in 300+ cities across India.

NGS Genetic TestAll Ages🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose Mirage Syndrome by detecting pathogenic mutations in the SAMD9 gene using NGS technology, enabling accurate clinical management and genetic counseling.

Test Code
5456
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
NGS Technology
Step 1

Sample Collection

Provide clinical history and undergo genetic counseling. No fasting required.

Method: Venipuncture

Step 2

Laboratory Analysis

Blood sample collected via venipuncture by trained phlebotomist.

Step 3

Report Delivery

Apply pressure to puncture site. Sample sent to lab for analysis.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling and clinical history review.
2
During the Test:Blood sample collection and NGS analysis.
3
After the Test:Report delivery and genetic counseling session.

About This Test

Who Should Get This Test

To diagnose Mirage Syndrome by detecting pathogenic mutations in the SAMD9 gene using NGS technology, enabling accurate clinical management and genetic counseling.

How to Prepare

  • Ensure proper identification
  • Use sterile equipment
  • Label samples correctly

Doctor's Notes

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

"Genetic testing for Mirage Syndrome is crucial for accurate diagnosis, management, and family planning. Early detection enables targeted care and genetic counseling."

Last medically reviewed: September 3, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5-10 mL
ContainerEDTA Vacutainer
Collection MethodVenipuncture

Sample Stability

Blood: 48 hours at 2-8°C
Extracted DNA: Stable at -20°C for long-term
Sample Rejection Criteria:
  • Hemolyzed sample
  • Insufficient volume
  • Improper labeling

Understanding Your Results

Results indicate presence or absence of pathogenic SAMD9 variants. Consult a geneticist for detailed interpretation.
Positive result: Pathogenic variant detected, confirm with clinical correlation
Negative result: No variants found, consider other diagnoses
Variant of uncertain significance: Further testing recommended
⚠️ When to Consult a Doctor:

If symptoms of Mirage Syndrome are present or there is a family history of genetic disorders.

Limitations

  • May not detect all genetic variants
  • Requires genetic counseling for interpretation
  • Not for prenatal diagnosis without validation

Risks & Considerations

  • Minimal physical risk from blood draw
  • Psychological impact of results
  • Privacy concerns with genetic data

Interfering Factors

  • Sample degradation
  • Contamination
  • Insufficient DNA quantity

Frequently Asked Questions

What is Mirage Syndrome?
Mirage Syndrome is a rare genetic disorder caused by mutations in the SAMD9 gene, leading to symptoms like intellectual disability, seizures, and growth issues.
What causes Mirage Syndrome?
It is caused by pathogenic mutations in the SAMD9 gene, which is inherited in an autosomal dominant pattern.
What are the symptoms of Mirage Syndrome?
Symptoms include intellectual disability, abnormal facial features, seizures, delayed development, growth retardation, skeletal abnormalities, and cardiovascular problems.
How is Mirage Syndrome diagnosed?
Diagnosis involves clinical evaluation and genetic testing, such as NGS to identify SAMD9 mutations.
What is the SAMD9 Gene Mirage Syndrome NGS Genetic Test?
It is a Next-Generation Sequencing test that analyzes the SAMD9 gene for mutations to confirm Mirage Syndrome diagnosis.
How much does the test cost?
The test costs INR 20000.0 at DNA Labs India, with home sample collection available.
What sample is required for the test?
A blood sample, extracted DNA, or one drop of blood on an FTA card is required.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings across India.
What is the accuracy of the test?
The NGS test is highly accurate for detecting SAMD9 gene mutations, but genetic counseling is recommended for interpretation.
Can the test be used for prenatal diagnosis?
No, this test is not validated for prenatal diagnosis; consult a geneticist for prenatal options.
What should I do if the test is positive?
Consult a geneticist or healthcare provider for management, genetic counseling, and family planning advice.
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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