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).
Tool call template
Replace each placeholder with a value matching the input schema. Only required parameters are included; add optional parameters as needed.
{
"id": 1,
"jsonrpc": "2.0",
"method": "tools/call",
"params": {
"arguments": {
"variant_ids": "<variant_ids>"
},
"name": "compare_variants"
}
}Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| variant_ids | Yes |