Assess the Significance of Genetic Variants with
Confidence, Control & Consistency

Improve quality, reduce error with Sunquest Mitogen™ Genetics

Assessing the clinical significance of novel variants is a sizable task –time-consuming, rife with data, and requires management and ranking of evidence amassed from multiple sources. Sunquest Mitogen™ Genetics helps you take control of this process by bringing order and consistency to the variant assessment process. With our capabilities, you can:


Access a robust information resource library, including ClinVar, PubMed, ExAC and gnomAD.


Process evidence against pre-loaded ACMG guidelines, using features such as visual cues and drag-and-drop functionality to guide your efforts in building evidence.


Benefit from a dynamic scoring algorithm that provides real-time calculation of a final compiled interpretation score with regard to pathogenicity.

Download the Product Brief Today!

Take control of the variant assessment process!

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