{"skill":{"slug":"variant-annotation-2","displayName":"Variant Annotation","summary":"Query and annotate gene variants from ClinVar and dbSNP databases. Trigger when: - User provides a variant identifier (rsID, HGVS notation, genomic coordinat...","tags":{"latest":"0.1.0"},"stats":{"comments":0,"downloads":256,"installsAllTime":0,"installsCurrent":0,"stars":0,"versions":1},"createdAt":1773394569768,"updatedAt":1777529292885},"latestVersion":{"version":"0.1.0","createdAt":1773394569768,"changelog":"Initial public release of variant-annotation skill.\n\n- Query and annotate gene variants using ClinVar and dbSNP databases, supporting inputs such as rsID, HGVS notation, and genomic coordinates.\n- Provides clinical significance (including ACMG guideline-based classification), allele frequencies, disease associations, and functional predictions.\n- Supports multiple input formats and batch annotation via CLI or Python API.\n- Includes detailed ACMG scoring system for pathogenicity assessment.\n- Integrates data from ClinVar, dbSNP, gnomAD, Ensembl VEP, and CADD.\n- For research/educational use only; not for clinical diagnostic purposes.","license":"MIT-0"},"metadata":{"os":null,"systems":null},"owner":{"handle":"ec-cyber258","userId":"publishers:ec-cyber258","displayName":"EC-cyber258","image":"https://avatars.githubusercontent.com/u/229709544?v=4"},"moderation":{"isSuspicious":true,"isMalwareBlocked":false,"verdict":"suspicious","reasonCodes":["suspicious.llm_suspicious"],"summary":"Detected: suspicious.llm_suspicious","engineVersion":"v2.4.5","updatedAt":1777529292885}}