clinvar-database
Utilities for querying the NCBI ClinVar database to retrieve variant records, clinical significance, and phenotype relationships; use when searching variants by gene/condition/significance, interpreting Pathogenic/Benign/VUS classifications, or annotating VCF files with ClinVar annotations.
What is this resource?
Utilities for querying the NCBI ClinVar database to retrieve variant records, clinical significance, and phenotype relationships; use when searching variants by gene/condition/significance, interpreting Pathogenic/Benign/VUS classifications, or annotating VCF files with ClinVar annotations.
Review the original project for installation steps, licenses, compatibility and updates. This directory provides discovery links, not downloadable or verified code.
Installation
For repositories supported by the Skills CLI, you can typically start with:
npx skills add aipoch/medical-research-skillsCheck the repository instructions and select the intended skill before installing. This command may not apply to every source.
Safety & attribution
This is an external resource, not independently security-audited by this directory. Inspect permissions, scripts and changes before using it with your files or accounts.