Find genetic variant details and IDs with dbSNP.
Retrieves short genetic variant annotations and maps between rsIDs, genomic coordinates, and HGVS expressions.
When to use it
Use to identify variants, retrieve variant summaries, convert rsIDs to coordinates, or survey a chromosomal region.
Give it an rsID, variant coordinates, HGVS expression, or chromosomal region; it saves the lookup results as JSON in /tmp/.
What you provide
Requires uv installed and on PATH, with setup directed through the uv skill.
The wrapper requires Python 3.10 or newer.
This skill
dbSNP
Looks up variants in dbSNP
uv
Sets up uv if needed