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We aim to streamline the rare disease treatment identification process. Input your disease and receive a collection of the most common CRISPR-targetable mutations. Skip deep searching; meet snoBANK.
An automated prioritization engine that takes a patient's VUSs and ranks the variant most likely to be pathogenic, showing exactly where it sits in the protein's structure.
Our technology. Your future. We strive to empower women to take control of their health, and explore their personalized treatment options using our comprehensive website.
