About
This skill enables programmatic querying of NCBI's ClinVar database to retrieve clinical significance data for genetic variants. Developers can use it to search by gene or position, interpret pathogenicity classifications, and annotate VCF files via the E-utilities API or FTP. It's designed for genomic medicine applications requiring variant interpretation and data integration.
Quick Install
Claude Code
Recommendednpx skills add overtimepog/AgentTheo -a claude-code/plugin add https://github.com/overtimepog/AgentTheogit clone https://github.com/overtimepog/AgentTheo.git ~/.claude/skills/clinvar-databaseCopy and paste this command in Claude Code to install this skill
GitHub Repository
Frequently asked questions
What is the clinvar-database skill?
clinvar-database is a Claude Skill by overtimepog. Skills package instructions and resources that Claude loads on demand, so Claude can perform clinvar-database-related tasks without extra prompting.
How do I install clinvar-database?
Use the install commands on this page: add clinvar-database to Claude Code as a plugin, or clone its repository into your skills directory, then restart Claude so it picks up the skill.
What category does clinvar-database belong to?
clinvar-database is in the Development category, tagged api and data.
Is clinvar-database free to use?
Yes. clinvar-database is listed on AIMCP and free to install. It runs inside Claude, so no separate service account is required to use the skill itself.
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