The collective knowledge of genetics continues to expand each year. As such, for patients who have been tested at PreventionGenetics, we will revisit a variant classification at no charge to provide the most current interpretation. Requests must be submitted through the Variant Interpretation Service in our portal, myPrevent. 

PreventionGenetics does not rely on informatics approaches alone to interpret sequence variants. We take a careful, expert, manual evaluation of the evidence—primarily published evidence—for an up-to-date scientific interpretation you can trust. 

PreventionGenetics has contributed many thousands of sequence variants to ClinVar and other public databases to advance genetic research and understanding for all, and continues to contribute as more and more variants are detected in our patients.