SKILL

clinvar-database

Query NCBI ClinVar for variant clinical significance. Search by gene/position, interpret pathogenicity classifications, access via E-utilities API or FTP, annotate VCFs, for genomic medicine.

Target: Databases. Automatically collected · unverified.

Use with Codex

A guide for this combination is not available yet, and compatibility has not been verified.

Requirements

Only the author’s Skill metadata is included. Read the full instructions to check dependencies, licensing and conditions of use.

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Read the author’s documentation ↗