Folklore Clinical Variant Interpretation MCP
Bioinformatics MCP for genomic variant interpretation, gene-disease evidence and literature.
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folklore.helena.bioAbout Folklore Clinical Variant Interpretation MCP
Folklore Clinical Variant Interpretation MCP is a hosted bioinformatics MCP service for public genomic variant evidence, literature and bounded gene–disease evidence. Version 1.5.0 provides six scientific tools plus a separate explicitly opt-in support_helena helper. Connect directly over stateless Streamable HTTP at https://api.helena.bio/folklore/v1/mcp with no account, API key or local runtime. Setup: https://folklore.helena.bio/integrations/mcp . Public integration repository: https://github.com/helena-bioinformatics/folklore-mcp . Supports public GRCh38 nuclear germline SNVs and simple indels under 50 bp. No patient, family, phenotype or private-case data, genomic files or batch uploads. Results require qualified professional review and are not a diagnosis or treatment recommendation. Apache-2.0 covers the public adapter, not the hosted backend or datasets.
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