biothings_get_variants
Retrieve annotation data for multiple specific variants using a comma-separated list of HGVS or rsIDs in a single request.
Instructions
Fetch multiple variants by a comma-separated list of HGVS or rsIDs.
Retrieves annotation data for **multiple specific variants** in a single request using their identifiers.
**This is the preferred tool over `query_many_variants` for fetching multiple specific variants when you already know
their standard IDs (HGVS or rsID).**
**Input Format:** Accepts a comma-separated list of variant IDs (HGVS or dbSNP rsIDs).
**Examples:** `variant_ids=chr7:g.140453134T>C,chr1:g.69511A>G` or `variant_ids=rs58991260,rs2500`
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| No | |||
| fields | No | all | |
| variant_ids | Yes |
Output Schema
| Name | Required | Description | Default |
|---|---|---|---|
| result | Yes |