Beta Thalassemia Full Gene Sequencing
Detects specific genetic mutations associated with beta thalassemia, a blood disorder that affects hemoglobin production. It helps diagnose and determine the severity of the condition.
Beta Thalassemia Full Gene Sequencing Test in Jalandhar Overview
No special preparations needed
- Specimen Source
- Preliminary Report
- Beta-thalassemia
The beta thalassemia mutation detection test identifies mutations in the HBB gene, responsible for beta thalassemia, a blood disorder that reduces hemoglobin production.
It is recommended for individuals with anemia, abnormal hemoglobin levels, or a family history of thalassemia.
A blood sample is analyzed using PCR or genetic sequencing to identify mutations in the HBB gene.
- Positive result: Confirms a beta thalassemia mutation.
- Negative result: No mutations detected in the HBB
Test code
2482
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 3 ML |
Specimen stability information
Edta Whole Blood
Specimen rejection criteria
Test run frequency
Every Day TIME - 09:30
Turn around time
12 Working Days
Performing locations
Department
- Advanced Molecular Diagnostics R&d
CPT and Loinc codes
Package price
₹7200
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₹7200