dbsnp-database

Maintained by google-deepmind

Use when you want to look up, map, and search for short genetic variants (SNPs, indels) in NCBI's dbSNP database. Resolves between rsIDs, genomic coordinates in VCF format, and HGVS strings. For an rsID, returns variant type, gene associations, clinical significance, allele frequencies, and genomic coordinates (GRCh38)

Current version: Unknown
License: Unknown
Network access: Unknown / not assessed
Review status: Not verified

Problem it solves

This catalog entry helps users find and evaluate dbsnp-database for the task described by its available catalog summary. Confirm the exact scope in the linked original source when one is available.

When to use it

Consider dbsnp-database when its available catalog summary matches the task at hand. When available, review the linked original source before use for precise instructions, requirements, and limitations.

dbsnp-database is listed as an agent skill in RefHub. The listed maintainer is google-deepmind. The available catalog summary is: Use when you want to look up, map, and search for short genetic variants (SNPs, indels) in NCBI's dbSNP database. Resolves between rsIDs, genomic coordinates in VCF format, and HGVS strings. For an rsID, returns variant type, gene associations, clinical significance, allele frequencies, and genomic coordinates (GRCh38) When available, review the linked original source for exact usage instructions, required tools, and limitations.

Installation and updates

These commands are displayed for copying only and are never executed on RefHub servers. Review the linked upstream source before running them.

Install command

npx skills add google-deepmind/science-skills --skill dbsnp-database -y

Agent compatibility

No compatibility test has been recorded

Do not assume agent compatibility until documented test evidence is available.