Detects mutations in the G6PD gene, commonly associated with G6PD deficiency, a condition leading to hemolytic anemia…. This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
G6PD deficiency (Coding Sequence Analysis)
22,644 THB
SKU :
MD-NLM006
Detects mutations in the G6PD gene, commonly associated with G6PD deficiency, a condition leading to hemolytic anemia.
Lab Categories : All Ages, EDTA Whole Blood, Fatigue, G6PD Deficiency, Genetic Disorder, Jaundice, Lab Test, PCR + DNA Sequencing
Diseases : G6PD Deficiency
Habits : Genetic Disorder
Age Groups : All Ages
Specimens : EDTA Whole Blood
Diagnostic Methods : DNA Sequencing, PCR
| Also Known As | G6PD Mutation Test |
|---|---|
| Specimen | EDTA whole blood >= 3 mL |
| Turnaround Time | 10 Days |
| Test Code | MD-NLM006 |
| Test Type | Special |
| Related Tests | Genetic Disorder Panel |
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