ClinVar is a public archive of information submitted by genetic testing labs on the relationships between medically important genetic variants and their clinical characteristics found in patients. Now, all variants, pathogenicity interpretations, and other key information within ClinVar’s database are included as part of Mastermind’s comprehensive body of evidence.

As a result, all users of Mastermind will be able to:

• Access all the scientific evidence for a variant required to support diagnostic decisions
• Search using any variant nomenclature rather than by a strict protocol, which can lead to missing evidence
• Streamline interpretation workflow within a single easily searchable interface-no need to navigate ClinVar separately

VIEW RESULTS IN CLINVAR

This information will be displayed at the top of your screen in a new tab next to our Curated Content (if available). In addition to seeing results from ClinVar, you will also have easy access to ongoing trials and treatment information for a growing list of diseases – and you can conveniently toggle between the two.

VIEW CURATED CONTENT AND INTERPRETATION

Start Searching the Most Comprehensive Source of Genomic Evidence

Not a Mastermind user yet? No problem. Make a free account here and start searching.