acmg-variant-classifier
// ACMG/AMP variant classification skill for systematic pathogenicity assessment
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updated:March 4, 2026
SKILL.mdreadonly
SKILL.md Frontmatter
nameacmg-variant-classifier
descriptionACMG/AMP variant classification skill for systematic pathogenicity assessment
allowed-toolsRead,Write,Glob,Grep,Edit,WebFetch,WebSearch,Bash
metadata[object Object]
ACMG Variant Classifier Skill
Purpose
Enable ACMG/AMP variant classification for systematic pathogenicity assessment following clinical guidelines.
Capabilities
- Automated evidence criteria application
- Population frequency filtering
- In silico prediction integration
- Literature evidence curation
- Inheritance pattern analysis
- Classification report generation
Usage Guidelines
- Apply ACMG criteria systematically
- Document evidence for each criterion
- Consider inheritance patterns in assessment
- Review literature for supporting evidence
- Generate clear classification reports
- Track classification changes over time
Dependencies
- InterVar
- VarSome API
- ClinVar
Process Integration
- Clinical Variant Interpretation (clinical-variant-interpretation)
- Rare Disease Diagnostic Pipeline (rare-disease-diagnostics)
- Newborn Screening Genomics (newborn-screening-genomics)