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This entry duplicates clinvar-database, which is the one we list in search.

clinvar-database

Use when needing clinical significance, pathogenicity classifications (e.g., Pathogenic, Benign, VUS), clinical evidence rationales, or finding "hard…

Skill by myoung906

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Install

Works with Claude Code, Claude apps, Codex, Cursor, Gemini CLI, GitHub Copilot, VS Code, OpenCode, Goose, Windsurf. Read the repository before you give any tool access to your data.

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About

Use when needing clinical significance, pathogenicity classifications (e.g., Pathogenic, Benign, VUS), clinical evidence rationales, or finding "hard positive" benchmark controls for human genomic variants.

Use cases: backend

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What's inside

Skill name
clinvar-database
Description
Use when needing clinical significance, pathogenicity classifications (e.g., Pathogenic, Benign, VUS), clinical evidence rationales, or finding "hard positive" benchmark controls for human genomic variants.
License
unknown
Instructions
364 lines in SKILL.md · view on GitHub

Before installing

  • Ships executable scripts

Files (3)

  • SKILL.md
  • citation.bib · references/
  • clinvar_api.py · scripts/

The license isn't open source, so the instructions aren't shown here. Read SKILL.md on GitHub

Signals

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Last commit (this folder)
Aug 17, 2026 (2 months ago)

From GitHub (fetched Oct 24, 2026).

Details

License
License unknown
First seen
Oct 24, 2026
Last checked
Oct 24, 2026

Same skill elsewhere

Copies of this SKILL.md published by others; search shows only one of them.

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Cite this page

clinvar-database skill. Agent Mart. https://agentmart.dev/skills/myoung906-clinvar-database (last updated 2026-10-24)