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folklore-variant-evidence

Retrieve ClinGen gene-disease validity assertions for a public gene or disease, and review source-linked public evidence and literature for one supported GRCh38 germline nuclear SNV or simple indel through Folklore Clinical Variant Interpretation MCP. Use when a scientific agent must branch deterministically on resolved, ambiguous, not-found, invalid, unsupported, or unavailable variant outcomes; chain a resolved public variant into related literature or publication details; or preserve evidence provenance without accepting patient, phenotype, family, segregation, or private case data.

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Install

npx research-agent-skills install folklore-variant-evidence
npx skills add KalarisLabs/research-agent-skills --skill folklore-variant-evidence

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When to use it

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Full playbook