clinvar-database
About
This skill enables developers to programmatically query NCBI's ClinVar database to retrieve clinical significance data for genetic variants. It supports searching by gene or position, interpreting pathogenicity classifications, and accessing data via the E-utilities API or FTP for tasks like VCF annotation. Use it to integrate variant clinical interpretations directly into genomic medicine applications and workflows.
Quick Install
Claude Code
Recommendednpx skills add Activer007/ordinary-claude-skills -a claude-code/plugin add https://github.com/Activer007/ordinary-claude-skillsgit clone https://github.com/Activer007/ordinary-claude-skills.git ~/.claude/skills/clinvar-databaseCopy and paste this command in Claude Code to install this skill
GitHub Repository
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