Alpha thalassemia Comprehensive (7 deletions and HBA1/HBA2 non-deletion)

Description

A comprehensive genetic test that detects common deletions and mutations associated with alpha thalassemia. This condition affects the production of hemoglobin, leading to anemia. The test is important for prenatal screening, family planning, and in populations where thalassemia is prevalent.

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.