clinvar-database
Query NCBI ClinVar for variant clinical significance. Search by gene/position, interpret pathogenicity classifications, access via E-utilities API or FTP, annotate VCFs, for genomic medicine.
Packaged view
This page reorganizes the original catalog entry around fit, installability, and workflow context first. The original raw source lives below.
Install command
npx @skill-hub/cli install microck-ordinary-claude-skills-clinvar-database
Repository
Skill path: skills_categorized/scientific-computing/clinvar-database
Query NCBI ClinVar for variant clinical significance. Search by gene/position, interpret pathogenicity classifications, access via E-utilities API or FTP, annotate VCFs, for genomic medicine.
Open repositoryBest for
Primary workflow: Ship Full Stack.
Technical facets: Full Stack, Backend.
Target audience: Development teams looking for install-ready agent workflows..
License: Unknown.
Original source
Catalog source: SkillHub Club.
Repository owner: Microck.
This is still a mirrored public skill entry. Review the repository before installing into production workflows.
What it helps with
- Install clinvar-database into Claude Code, Codex CLI, Gemini CLI, or OpenCode workflows
- Review https://github.com/Microck/ordinary-claude-skills before adding clinvar-database to shared team environments
- Use clinvar-database for development workflows
Works across
Favorites: 0.
Sub-skills: 0.
Aggregator: No.