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).
How to install dbsnp_database?
google-deepmind/science-skills/dbsnp_database
$npx -y skills add google-deepmind/science-skills --skill dbsnp_databaseInstalls into the current project.
›Prefer a prompt? Paste this to your agent
Run `npx skills use "https://github.com/google-deepmind/science-skills" --skill "google-deepmind/science-skills/dbsnp_database"` and follow the generated skill instructions now. Read its complete output, redirecting it to a temporary file first if necessary. Resolve relative paths from the supporting-files directory it provides.
Use the skills in "https://github.com/google-deepmind/science-skills" that are relevant to the current task. Run `npx skills add "https://github.com/google-deepmind/science-skills"` and select the relevant skills, then follow their instructions.
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