A powerful clinical-grade test sequencing all protein-coding genes (exome) to identify genetic mutations responsible for inherited or rare disorders. Analyzes over 20,000 genes to detect clinically significant variants influencing health, development, and disease susceptibility.
Who it’s for: Individuals with complex, unexplained, or inherited health conditions seeking precision diagnostics.
Whole Exome Sequencing sequences the protein-coding regions of the genome (the exome) to identify genetic variants responsible for complex, rare, or undiagnosed medical conditions.
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