{"skill":{"slug":"variant-annotation","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":{"Gene":"1.0.0","Variant":"1.0.0","latest":"1.0.0"},"stats":{"comments":0,"downloads":435,"installsAllTime":1,"installsCurrent":0,"stars":0,"versions":1},"createdAt":1772265678991,"updatedAt":1777525466890},"latestVersion":{"version":"1.0.0","createdAt":1772265678991,"changelog":"Initial release of the variant-annotation skill for clinical variant interpretation.\n\n- Query and annotate variants using ClinVar, dbSNP, and population frequency data.\n- Supports multiple input formats: rsID, HGVS notation, genomic coordinates, VCF.\n- Provides clinical significance, ACMG guideline-based classification, allele frequencies, disease associations, and functional predictions.\n- Python API and CLI interfaces for individual and batch variant annotation.\n- Implements ACMG scoring and variant classification thresholds.\n- Integrates major datastores (ClinVar, dbSNP, gnomAD, Ensembl VEP, CADD) for comprehensive annotation.","license":null},"metadata":{"os":null,"systems":null},"owner":{"handle":"aipoch-ai","userId":"s17fjw78yq6wtd4ep6zsaxwrn983hznr","displayName":"AIpoch","image":"https://avatars.githubusercontent.com/u/258999481?v=4"},"moderation":{"isSuspicious":true,"isMalwareBlocked":false,"verdict":"suspicious","reasonCodes":["suspicious.llm_suspicious","suspicious.vt_suspicious"],"summary":"Detected: suspicious.llm_suspicious, suspicious.vt_suspicious","engineVersion":"v2.4.5","updatedAt":1777525466890}}