Sharing information about variants is one of the most powerful tools we have to improve the accuracy of genomic data interpretation. But how do we make this work at scale?

The agenda features experiences from well-established platforms including Shariant, Clinical Variant Ark, and the All4One Health Data Ecosystem, as well as tools to facilitate variant matching across platforms. After presentations, a discussion period will provide participants with an opportunity to identify synergies, learn more about existing tools built on GA4GH standards, and explore how to build upon these efforts nationally and internationally.