ANKRD26 Gene Thrombocytopenia type 2 NGS Genetic Test
Short Name: ANKRD26 Thrombocytopenia Type 2 NGS Test
Also known as: ANKRD26-related thrombocytopenia, Inherited thrombocytopenia type 2
ANKRD26 Gene Thrombocytopenia type 2 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS), Genetic Sequencing 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
The purpose of the ANKRD26 Gene Thrombocytopenia Type 2 NGS Genetic Test is to identify mutations in the ANKRD26 gene that cause inherited thrombocytopenia. This test provides a definitive diagnosis, helps in carrier identification, guides treatment decisions, and supports family planning and genetic counseling.
- Test Code
- 2692
- 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), Genetic Sequencing
Sample Collection
Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with ANKRD26-related thrombocytopenia.
Method: Venipuncture
Laboratory Analysis
Standard blood draw procedure using venipuncture. For FTA card, a drop of blood is applied.
Report Delivery
Sample is processed for DNA extraction and NGS analysis. Results are reviewed by geneticists.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the ANKRD26 Gene Thrombocytopenia Type 2 NGS Genetic Test is to identify mutations in the ANKRD26 gene that cause inherited thrombocytopenia. This test provides a definitive diagnosis, helps in carrier identification, guides treatment decisions, and supports family planning and genetic counseling.
How to Prepare
- Provide detailed clinical history.
- Undergo genetic counseling for pedigree analysis.
- Ensure proper sample labeling and handling.
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is crucial for diagnosing inherited thrombocytopenia, guiding treatment, and family planning. Early detection can prevent complications from excessive bleeding."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Insufficient sample volume
- Improperly labeled sample
Understanding Your Results
Positive (Mutation Detected)
Confirms diagnosis of ANKRD26-related Thrombocytopenia Type 2. Genetic counseling and family screening recommended.
Negative (No Mutation Detected)
No pathogenic variants identified in the ANKRD26 gene. Clinical symptoms may require further evaluation for other causes of thrombocytopenia.
Variant of Uncertain Significance (VUS)
A genetic variant was found, but its clinical significance is unknown. Further testing and clinical correlation are advised.
Consult a hematologist or genetic counselor if you experience symptoms of thrombocytopenia, have a family history of the condition, or for preconception genetic counseling.
Limitations
- ⚠Test may not detect all genetic variants; clinical correlation is required.
- ⚠Results should be interpreted in conjunction with clinical findings and family history.
Risks & Considerations
- ●Minimal risks from blood draw, such as bruising or infection at the puncture site.
- ●No significant risks from the genetic test itself.
Interfering Factors
- ●Sample contamination
- ●Hemolyzed blood sample
- ●Improper sample storage
Compare With Similar Tests
| Test | ANKRD26 Gene Thrombocytopenia type 2 NGS Genetic Test | Complete Blood Count (CBC) | Platelet Function Test | Bone Marrow Biopsy | Other Genetic Panels for Thrombocytopenia |
|---|---|---|---|---|---|
| Comparison | ANKRD26 Gene Thrombocytopenia type 2 NGS Genetic Test | Measures platelet count but does not identify genetic cause. | Assesses platelet function, not genetic mutations. | Evaluates bone marrow production but is invasive; genetic test is non-invasive. | May include multiple genes; this test is specific to ANKRD26. |
Frequently Asked Questions
What is ANKRD26 Gene Thrombocytopenia Type 2?
What are the symptoms of ANKRD26-related Thrombocytopenia?
How is ANKRD26 Thrombocytopenia diagnosed?
What is the cost of the ANKRD26 Gene Thrombocytopenia Type 2 NGS Genetic Test?
Is the NGS Genetic Test invasive?
How long does it take to get the test results?
Can this test identify carriers of the condition?
What should I do if the test is positive?
Is genetic counseling required before the test?
Are there any risks associated with the test?
Is the test covered by insurance?
How can I book the test?
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