Genomenon Integrates ClinVar Data into Mastermind to Support Clinical Decision-Making – EIN News

Patient Variant Information Submitted to NIH Now Accessible Through Mastermind Genomic Search Engine

ANN ARBOR, Mich., Sept. 7, 2022 /PRNewswire-PRWeb/ — Genomenon, Inc., an AI-driven genomics company, has integrated all the variants and pathogenicity interpretations from the ClinVar database into the Mastermind Genomic Search Engine. This integration combines patient variants found by genetic testing labs and submitted to ClinVar with the scientific evidence for these variants found across the entirety of medical literature, all in a single Mastermind search.

ClinVar is a public archive of data submitted by genetic testing labs on the relationships between medically important genetic variants and their clinical characteristics found in patients. Sponsored by the National Institutes of Health (NIH), ClinVar is widely used by genomic analysts involved in clinical variant interpretation—a process that identifies disease-causing genetic variants in patient DNA to help clinicians make…

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