SAMD9 Gene Mirage syndrome NGS Genetic Test
Short Name: SAMD9 Gene Test for Mirage Syndrome
Also known as: Mirage Syndrome, SAMD9 Gene Mutation Disorder
SAMD9 Gene Mirage syndrome 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 identify mutations in the SAMD9 gene associated with Mirage syndrome for diagnostic confirmation, risk evaluation, and clinical management.
- Test Code
- 2174
- 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
A genetic counseling session is recommended to discuss the test, draw a pedigree chart, and understand implications. No specific preparation is required.
Laboratory Analysis
Blood sample will be collected via venipuncture, or a saliva/FTA card sample may be used as per laboratory protocol.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Resume normal activities.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the SAMD9 gene associated with Mirage syndrome for diagnostic confirmation, risk evaluation, and clinical management.
How to Prepare
- Ensure proper identification and labeling of the sample
- Follow instructions for blood, saliva, or FTA card collection
- Transport the sample to the lab at ambient temperature as specified
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early genetic testing for Mirage syndrome is crucial for accurate diagnosis, personalized management, and family planning counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed, clotted, or insufficient sample volume
- Sample improperly labeled or contaminated
- Sample received in damaged container
Understanding Your Results
Pathogenic SAMD9 mutation detected, consistent with Mirage syndrome diagnosis. Clinical correlation and family studies recommended.
Result type: Positive
No pathogenic mutations identified in the SAMD9 gene. Consider other genetic or clinical evaluations if symptoms persist.
Result type: Negative
A genetic variant was found but its clinical significance is unknown. Further testing and follow-up may be needed.
Result type: Variant of Uncertain Significance
Consult a doctor if genetic test results are positive, if there is a family history of Mirage syndrome, or if symptoms such as tumors, developmental delays, or seizures are present.
Limitations
- ⚠May not detect all types of genetic variants, such as large deletions or duplications
- ⚠Variants of uncertain significance may be identified, requiring further evaluation
- ⚠Does not rule out other genetic conditions with overlapping symptoms
Risks & Considerations
- ●Minimal risks associated with blood draw, such as pain, bruising, or infection
- ●Psychological impact of genetic results, including anxiety or stress
Interfering Factors
- ●Sample contamination or degradation
- ●Hemolyzed or lipemic blood samples
- ●Incorrect sample storage or handling
Frequently Asked Questions
What is Mirage syndrome?
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What is the cost of the SAMD9 Gene Mirage Syndrome NGS Genetic Test?
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Is home sample collection available?
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Reference Laboratory Services
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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✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
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