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.
Install
npx skills add K-Dense-AI/scientific-agent-skills --skill folklore-variant-evidencenpx skills add K-Dense-AI/scientific-agent-skills --skill folklore-variant-evidence -a claude-code -gnpx skills add K-Dense-AI/scientific-agent-skills --skill folklore-variant-evidence -a codex -ggemini skills install https://github.com/K-Dense-AI/scientific-agent-skills.git --path skills/folklore-variant-evidencegh skill install K-Dense-AI/scientific-agent-skills folklore-variant-evidencegit clone --depth 1 https://github.com/K-Dense-AI/scientific-agent-skills /tmp/K-Dense-AI__scientific-agent-skills
mkdir -p ~/.claude/skills ~/.agents/skills
cp -R /tmp/K-Dense-AI__scientific-agent-skills/skills/folklore-variant-evidence ~/.claude/skills/folklore-variant-evidence # Claude Code
cp -R /tmp/K-Dense-AI__scientific-agent-skills/skills/folklore-variant-evidence ~/.agents/skills/folklore-variant-evidence # Codex, Cursor, Gemini CLI, Copilot, OpenCode