AI & Machine Learning
Folklore Variant Evidence
Retrieves ClinGen gene-disease validity assertions for a public gene or disease, and reviews source-linked public evidence and literature for one supported GRCh38 germline nuclear SNV or simple indel through Folklore Clinical Variant Interpretation MCP. Used 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.
- Publisher / source
- Scientific Agent Skills
- Upstream record
- K-Dense-AI/scientific-agent-skills
- Version
- Version 4
- Published
- Publication review
- Approved for publication
- Content fingerprint
134b5ea684815b99c56fadf92a1cb42d37eaca4245515278e404b8876b7acfe0