Data Science & Analytics
dbSNP Database
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).
- Publisher / source
- google-deepmind/science-skills (found on skills.sh)
- Upstream record
- google-deepmind/science-skills
- Version
- Version 3
- Published
- Publication review
- Approved for publication
- Content fingerprint
261817ea3ca4ff6396b49902c8004a44b6d0a7fdc7620d1212ecfe3ede21e80e