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.
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tessl review fix ./skills/clinvar_database/SKILL.mdThe skill exposes the agent to untrusted, user-generated content from public third-party sources, creating a risk of indirect prompt injection. This includes browsing arbitrary URLs, reading social media posts or forum comments, and analyzing content from unknown websites.
The workflow queries the NCBI ClinVar database via E-utilities APIs, ingesting third-party clinical submissions, curator notes, and free text associated with genomic variants.
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