Look up short genetic variants like SNPs and indels in the NCBI dbSNP database. You can search using an rsID, genomic coordinates, or an HGVS string. The skill returns variant type, gene associations, clinical significance, and population allele frequencies.
It also maps between different identifier formats. For example, you can turn a coordinate into a canonical rsID or convert an rsID back to coordinates on the GRCh38 assembly. This is useful for researchers and anyone working with genetic data.
Rate limits apply but you can optionally add a free NCBI API key to increase speed. The skill handles retries and JSON parsing automatically for a smooth experience.
Global
mkdir -p ~/.claude/skills/dbsnp-databaseProject
mkdir -p .claude/skills/dbsnp-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