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. With a database of more than 187,000 pieces of evidence across 125,000 genetic variants that is continually updated with data from the latest functional studies, MAVEvidence allows clinical geneticists to leverage cutting-edge research without the headaches of manually searching and analyzing large and complex datasets. 

Check out the user guide, sign up for an account, and start using MAVEvidence today.

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