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.
How to install clinvar_database?
google-deepmind/science-skills/clinvar_database
$npx -y skills add google-deepmind/science-skills --skill clinvar_databaseInstalls into the current project.
›Prefer a prompt? Paste this to your agent
Run `npx skills use "https://github.com/google-deepmind/science-skills" --skill "google-deepmind/science-skills/clinvar_database"` and follow the generated skill instructions now. Read its complete output, redirecting it to a temporary file first if necessary. Resolve relative paths from the supporting-files directory it provides.
Use the skills in "https://github.com/google-deepmind/science-skills" that are relevant to the current task. Run `npx skills add "https://github.com/google-deepmind/science-skills"` and select the relevant skills, then follow their instructions.
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