get_genetic_variants
Search ClinVar for genetic variants associated with a gene. Get clinical significance, conditions, and review status from NCBI ClinVar.
Tool call template
This tool declares no required parameters. Add optional parameters from the input schema as needed.
{
"id": 1,
"jsonrpc": "2.0",
"method": "tools/call",
"params": {
"arguments": {},
"name": "get_genetic_variants"
}
}Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| gene | No | Gene symbol (default: BRCA1) | BRCA1 |
| limit | No | Number of variants (max 25, default 10) | |
| significance | No | pathogenic, benign, or uncertain | pathogenic |