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.
MAVEvidence allows clinical geneticists to leverage cutting-edge research without the headaches of manually searching for and analyzing large and complex datasets.
Next-Level Genetic Variant Analysis
200,000 pieces of evidence
125,000 genetic variants
Used by clinicians and scientists at
