compare_variants
Enables side-by-side comparison of multiple variants, displaying clinical label, pathogenicity score, and top disruption. Use to rank or contrast variants efficiently.
Instructions
Compare multiple variants side-by-side.
Fetches clinical label, pathogenicity score, gene, HGVS protein, consequence, and the top-1 disruption for each. Use when the user asks to contrast, rank, or compare 2+ variants, instead of looping get_variant.
Args: variant_ids: List of variant IDs in chr:pos:ref:alt format (max 10).
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| variant_ids | Yes |