runchuan-bu/bioclaw/query-clinvar
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Query ClinVar for clinical variant significance. Use when user asks about variant pathogenicity, genetic variants, clinical significance, or disease-causing mutations. Triggers on "clinvar", "pathogenic", "variant significance", "clinical significance", "disease variant", "mutation pathogenicity".
Install
npx vskill@latest install runchuan-bu/bioclaw/query-clinvarSKILL.md
ClinVar Clinical Variant Database
Query NCBI ClinVar for clinical significance of genetic variants.
When to Use
- User asks if a variant is pathogenic
- User wants to find known pathogenic variants in a gene
- User asks about clinical significance of SNPs
- User wants variant-disease associations
How to Execute
Common Search Patterns
- Pathogenic variants in gene:
BRCA1[gene] AND clinsig_pathogenic[prop] - By rsID:
rs6025[rsid] - By disease:
"breast cancer"[dis] AND clinsig_pathogenic[prop] - By chromosome region:
17[chr] AND 43000000:44000000[chrpos37] - Germline variants:
BRCA1[gene] AND origin_germline[prop]
Clinical Significance Categories
- Pathogenic, Likely pathogenic, Uncertain significance, Likely benign, Benign
Follow-up Suggestions
- "Want me to check the allele frequency in gnomAD?"
- "Should I look up this variant in Ensembl for more context?"
- "Want me to find all pathogenic variants in this gene?"
Security
- Security scanPassed, 100 of 100Pattern checks on the skill's files.
- Model reviewNot runA model review is scheduled for the next rescan.
Quality evaluation
- Task evaluationNot runNo evaluation yet. Run one in Skill Studio.
Source
- SKILL.md in the repositoryCheckingcontainer/skills/query-clinvar/SKILL.md
Popularity
- Repository stars
- 384
- Repository forks
- 48
- 7-day trend score
- 30
Stars and forks are for the whole GitHub repository, not this skill alone. Not refreshed yet.
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