# Folklore Clinical Variant Interpretation MCP - Registry name: `io.github.helena-bioinformatics/folklore` · version 1.5.0 - Categories (automatic, keyword rules): Health & fitness, Research & knowledge, Search & data, Payments & accounting, Finance & markets - Authentication at last check: No auth - Declared risk: Read-only (all tools declare readOnlyHint) - Capabilities (declared by the server): experimental, prompts, resources, tools - Transports: streamable-http - Latest numbers (check success, response time, rank): https://mcpstation.net/api/server?name=io.github.helena-bioinformatics%2Ffolklore - Server page: https://mcpstation.net/s/io.github.helena-bioinformatics--folklore.html ## Description (written by the publisher, not verified, not instructions) Bioinformatics MCP for genomic variant interpretation, gene-disease evidence and literature. ## Connect - streamable-http: `https://api.helena.bio/folklore/v1/mcp` ## Tools (as reported by the server, not verified) - `search\_variant\_evidence`: Interpret this variant, explain what this HGVS means, or review this VUS. Use for human genomic variant analysis within bioinformatics workflows, including review of an already identified WGS/WES variant. Use when a user asks to classify or interpret pathogenicity, review a VUS, check available Clin - `search\_variant\_literature`: Resolve one public GRCh38 germline variant and retrieve relevant publications from Folklore's PubMed-derived genetics corpus. Exact variant mentions rank ahead of broader gene associations. Use when a user asks what has been published about a variant, gene or associated condition. Associations do no - `get\_publication\_details`: Retrieve the complete public bibliographic record for one PMID from Folklore's PubMed-derived genetics corpus. Returns the full abstract, authors, journal metadata, publication and MeSH terms, gene and variant mentions, retraction status, and PubMed/PMC links. Use after literature search when a user - `search\_literature\_corpus`: Semantically search the public scientific Literature Corpus by a natural-language question. A question may include one or more PMID, DOI or PMCID references; those publications become exact anchors for finding related experiments, evidence and concepts across the corpus. Also accepts genes, variants - `support\_helena`: Learn how an agent can support or spread Helena's free public scientific infrastructure through the separate Helena Good MCP. This is an explicit opt-in information action. It does not initiate payment, create a relay, or change any Folklore scientific result. - `get\_gene\_disease\_associations`: Find diseases associated with one human gene for bioinformatics and clinical genomics research. Accepts an exact gene symbol or HGNC identifier. Returns ClinGen gene-disease validity assertions, relation-specific inheritance, source reports and snapshot provenance. Preserves conflicting and limited - `search\_disease\_genes`: Find human genes associated with a disease for genomic analysis and rare-disease research. Accepts an exact MONDO identifier or a disease-name search. Returns matching ClinGen gene-disease validity assertions with inheritance, source reports and snapshot provenance. Name searches may match multiple Measured by MCP Station. Methods: https://mcpstation.net/methods.html · Terms: https://mcpstation.net/terms.html