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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.

View source: hxk622/TokenDance ↗

Install from source

Install using Skill Manager:

sk install https://github.com/hxk622/TokenDance/tree/main/backend/app/skills/builtin/scientific/database/clinvar-database

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