get_genetic_variants
Search ClinVar for genetic variants associated with a gene. Get clinical significance, conditions, and review status from NCBI ClinVar.
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 |