clinvar-database
Description
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.
How to Use
- Visit the GitHub repository to get the SKILL.md file
- Copy the file to your project root or .cursor/rules directory
- Restart your AI assistant or editor to apply the new skill
Tags
About clinvar-database
clinvar-database is an AI skill in the ml-data category, designed to help developers and users work more effectively with AI tools. 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.
This skill has earned 2,800 stars on GitHub, reflecting strong community adoption and trust. It is compatible with claude.
Key Capabilities
Why Use clinvar-database
Adding clinvar-database to your AI workflow can significantly enhance your productivity in ml-data tasks. With pre-defined prompt templates and best practices, this skill helps AI assistants better understand your requirements and deliver more accurate responses.
Whether you use claude, you can easily integrate this skill into your existing development environment.
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