ClinVar is a database that collects the clinical meaning of human genetic changes. It tells you if a variant is Pathogenic, Benign, or uncertain. This helps researchers and doctors find the truth about genetic variants.
You can search for a specific variant and see its star rating and supporting evidence. The data comes from laboratories around the world. Use it to find benchmark controls or check conflicting interpretations.
This tool is for anyone working with human genetic data. It gives you the ground truth for clinical classifications.
Global
mkdir -p ~/.claude/skills/clinvar-databaseProject
mkdir -p .claude/skills/clinvar-databaseSource Repository
Healthcare Emr Patternsaffaan-m/everything-claude-code
Build safe efficient healthcare EMR systems with proven clinical patterns
Healthcare Cdss Patternsaffaan-m/everything-claude-code
Build patient safety critical CDSS modules with zero tolerance for false negatives
Mfds Food Safetynomadamas/k-skill
Ask about food safety but it interviews you first for symptoms
Mfds Drug Safetynomadamas/k-skill
Check drug safety with official data after a mandatory interview about symptoms
Healthkitdpearson2699/swift-ios-skills
Easily read write and query Apple Health data for health and fitness apps
Sensorkitdpearson2699/swift-ios-skills
Gather sensor data from iOS devices for approved health research studies
Ggetaffaan-m/everything-claude-code
Quick genomic database queries and reproducible bioinformatics lookups with gget
Single Cell Rna Qcanthropics/knowledge-work-plugins
Automatically filter low-quality cells from single-cell RNA-seq data using scverse best practices