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Disclaimer: This sample document is the work product of the N=1 Collaborative. This document is intended to assist clinicians, scientists, and healthcare professionals with resources featuring publicly available tools to assist in evaluating genetic variants for their ASO eligibility. This document, shared by collaborating organizations, is intended for research and educational purposes only. The information is based on the best available knowledge and practice at the time of publication. The N1C reserves the right to update, modify, or withdraw these practices at any time without prior notice. Users of these documents should exercise their own judgment and discretion in applying these practices to their specific situations.