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.
安装
npx skills add davila7/claude-code-templates --skill clinvar-databasenpx skills add davila7/claude-code-templates --skill clinvar-database -a claude-code -gnpx skills add davila7/claude-code-templates --skill clinvar-database -a codex -ggemini skills install https://github.com/davila7/claude-code-templates.git --path cli-tool/components/skills/scientific/clinvar-databasegh skill install davila7/claude-code-templates clinvar-databasegit clone --depth 1 https://github.com/davila7/claude-code-templates /tmp/davila7__claude-code-templates
mkdir -p ~/.claude/skills ~/.agents/skills
cp -R /tmp/davila7__claude-code-templates/cli-tool/components/skills/scientific/clinvar-database ~/.claude/skills/clinvar-database # Claude Code
cp -R /tmp/davila7__claude-code-templates/cli-tool/components/skills/scientific/clinvar-database ~/.agents/skills/clinvar-database # Codex, Cursor, Gemini CLI, Copilot, OpenCode