get_variant_info
Fetch detailed variant information from Ensembl using rsID, including genomic position, alleles, clinical significance, and functional consequences.
Instructions
Get detailed variant/SNP information from Ensembl by rsID. Returns position, alleles, clinical significance, and consequences.
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| rsid | Yes | dbSNP rsID (e.g., 'rs1234567') |