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.
63
75%
Does it follow best practices?
Run evals on this skill
Adds up to 20 points to the overall score
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Low
Low-risk findings worth noting
Fix and improve this skill with Tessl
tessl review fix ./skills/clinvar_database/SKILL.mdLoading evals
0b42509
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