clinvar_findings
Retrieves pathogenic or likely-pathogenic ClinVar variants carried in a consumer DNA report, including plausibility confidence and flags for disease-risk or carrier-status questions.
Instructions
ClinVar scan results (pathogenic / likely-pathogenic alleles carried, with plausibility confidence and flags). Health-sensitive: call only when the user asks about disease risk or carrier status.
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": "clinvar_findings"
}
}Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| report_dir | No |