MAVEvidence is the premier functional evidence resource for the clinical genetics community. MAVEvidence delivers increased productivity and time savings through comprehensive curation, rigorous analysis, and clear presentation of functional evidence derived from high-throughput studies of genetic variants. The MAVEvidence platform contains more than 186,000 pieces of evidence across 124,000 genetic variants, and is continually updated with data from the latest functional studies.

Check out the MAVEvidence page to learn more.