SLC4A1 Gene Ovalocytosis NGS Genetic Test
Short Name: SLC4A1 Ovalocytosis Test
Also known as: Hereditary Ovalocytosis, SLC4A1-related Ovalocytosis
SLC4A1 Gene Ovalocytosis 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 Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
To identify pathogenic mutations in the SLC4A1 gene associated with ovalocytosis, aiding in diagnosis and management.
- Test Code
- 2636
- 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
Genetic counseling is recommended to understand the implications of the test.
Method: Venipuncture or FTA card collection
Laboratory Analysis
A blood sample is drawn from a vein or collected via FTA card.
Report Delivery
The sample is sent to the laboratory for NGS analysis.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify pathogenic mutations in the SLC4A1 gene associated with ovalocytosis, aiding in diagnosis and management.
How to Prepare
- Provide clinical history of the patient
- Draw a pedigree chart of family members affected
- Ensure proper sample labeling
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Genetic testing for SLC4A1 mutations is crucial for diagnosing ovalocytosis and guiding management. Early detection can help in monitoring and treatment."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Insufficient sample volume
- Improperly labeled sample
Understanding Your Results
If you experience symptoms of anemia or have a family history of ovalocytosis, consult a geneticist or hematologist.
Limitations
- ⚠May not detect all types of mutations
- ⚠Variants of uncertain significance may be reported
- ⚠Does not rule out other genetic conditions
Risks & Considerations
- ●Minor bruising at the blood draw site
- ●Rare risk of infection
- ●Emotional impact of genetic results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Hemolyzed blood sample
Compare With Similar Tests
| Test | SLC4A1 Gene Ovalocytosis NGS Genetic Test | Complete Blood Count (CBC) | Hemoglobin Electrophoresis |
|---|---|---|---|
| Comparison | SLC4A1 Gene Ovalocytosis NGS Genetic Test |
Frequently Asked Questions
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