Data & ReproClinical MedicineFreedomIntelligence/OpenClaw-Medical-SkillsData & Reproduction
CL

clinical-interpretation

Maintainer FreedomIntelligence · Last updated April 1, 2026

clinical-interpretation.

OpenClawNanoClawAnalysisReproductionclinical-interpretationopenclaw medical skillsadditional scientific toolsclinical

Original source

FreedomIntelligence/OpenClaw-Medical-Skills

https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/clinical-interpretation

Maintainer
FreedomIntelligence
License
MIT
Last updated
April 1, 2026

Skill Snapshot

Key Details From SKILL.md

2 min

Key Notes

  • Prioritize and interpret variants for clinical significance using databases and ACMG/AMP guidelines.

Source Doc

Excerpt From SKILL.md

Exclude benign

bcftools view -e 'INFO/CLNSIG~"Benign" || INFO/CLNSIG~"Likely_benign"'
with_clinvar.vcf.gz -Oz -o not_benign.vcf.gz


## ClinVar Significance Levels

| CLNSIG | Meaning | Action |
|--------|---------|--------|
| Pathogenic | Disease-causing | Report |
| Likely_pathogenic | Probably disease-causing | Report with caveat |
| Uncertain_significance | VUS | May report, needs follow-up |
| Likely_benign | Probably not disease-causing | Usually exclude |
| Benign | Not disease-causing | Exclude |
| Conflicting | Multiple interpretations | Manual review |

## ClinVar Review Status

| CLNREVSTAT | Stars | Meaning |
|------------|-------|---------|
| practice_guideline | 4 | Expert panel reviewed |
| reviewed_by_expert_panel | 3 | ClinGen expert reviewed |
| criteria_provided,_multiple_submitters | 2 | Consistent assertions |
| criteria_provided,_single_submitter | 1 | One submitter with criteria |
| no_assertion_criteria | 0 | No criteria provided |

```bash

Use cases

  • Use clinical-interpretation for clinical, translational, or medical research tasks.
  • Apply clinical-interpretation when healthcare-specific guidance is required.

Not for

  • Do not rely on this catalog entry alone for installation or maintenance details.

Upstream Related Skills

  • variant-calling/variant-annotation - VEP/SnpEff annotation
  • variant-calling/filtering-best-practices - Quality filtering
  • database-access/entrez-fetch - Download ClinVar/OMIM data
  • pathway-analysis/go-enrichment - Gene set analysis

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