clinvar-database
•published 2026/02/01
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.
📦 Install Skill
Command line install
Install directly with the `skills` CLI.
npx skills add x-cmd/skill/data/k-dense-ai/clinvar-databaseFile Explorer
No file selected
Select a file to view its content