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).
安装
尚未确认此技能的独立目录。下面命令会打开仓库技能选择器，请按上游说明选择技能。
skills CLI
npx skills add google-deepmind/science-skills