RUNX1 Gene Leukemia, acute myeloid NGS Genetic Test
Short Name: RUNX1 AML NGS Test
Also known as: RUNX1-associated AML, RUNX1 mutation leukemia
RUNX1 Gene Leukemia, acute myeloid 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.
🩺 Medically Reviewed By
Dr SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician · Reg: 8052
Last reviewed: September 7, 2026
Overview
To identify mutations in the RUNX1 gene for diagnosis and personalized treatment of acute myeloid leukemia.
- Test Code
- 2884
- 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
Sample Collection
No special preparation required. Provide clinical history and undergo genetic counseling if needed.
Method: Venipuncture or FTA Card
Laboratory Analysis
Blood sample will be drawn by a trained phlebotomist using sterile equipment.
Report Delivery
Apply pressure to the puncture site to prevent bleeding. Sample will be processed in the laboratory.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the RUNX1 gene for diagnosis and personalized treatment of acute myeloid leukemia.
How to Prepare
- Use sterile collection tubes
- Label samples with patient details
- Transport at ambient room temperature
- Avoid hemolysis during blood draw
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"Early genetic testing for RUNX1 mutations can guide personalized treatment in acute myeloid leukemia, improving patient outcomes."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Incorrect labeling or missing information
Understanding Your Results
Positive
Pathogenic variant detected in RUNX1 gene, associated with increased risk of AML. Consult oncologist for treatment options.
Negative
No pathogenic variants detected. Clinical correlation recommended if symptoms persist.
Variant of Uncertain Significance
Genetic variant found but significance unclear. Further testing or family studies may be needed.
If symptoms of leukemia persist, if genetic counseling is needed, or if results indicate a pathogenic variant.
Limitations
- ⚠May not detect all RUNX1 mutations
- ⚠Results require clinical correlation
- ⚠Not suitable for prenatal diagnosis
Risks & Considerations
- ●Minor bruising at puncture site
- ●Rare risk of infection
- ●Emotional impact of results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA quality
- ●Previous treatments affecting DNA integrity
Compare With Similar Tests
| Test | RUNX1 Gene Leukemia, acute myeloid NGS Genetic Test | Sanger Sequencing | FISH Analysis |
|---|---|---|---|
| Comparison | RUNX1 Gene Leukemia, acute myeloid NGS Genetic Test |
Frequently Asked Questions
What is RUNX1 Gene Leukemia?
What are the symptoms of RUNX1 gene leukemia?
How is RUNX1 gene leukemia diagnosed?
What is the cost of NGS Genetic Test for RUNX1 gene leukemia?
How long does it take to get results?
Is home sample collection available?
What does a positive result mean?
Can this test be used for treatment planning?
Are there any risks associated with the test?
How accurate is the NGS Genetic Test?
What should I do before getting tested?
Is genetic counseling recommended?
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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.
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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