clinical-variant-reporter
Classifies germline variants using ACMG/AMP guidelines, generating clinical-grade reports with evidence audit trails.
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The clinical-variant-reporter skill was audited on Jun 11, 2026 and we found 8 security issues across 1 threat category. Review the findings below before installing.
Categories Tested
Security Issues
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External URL reference
SourceSKILL.md
| 227 | - [Richards et al. (2015)](https://pubmed.ncbi.nlm.nih.gov/25741868/) — ACMG/AMP standards and guidelines for the interpretation of sequence variants. *Genet Med* 17:405–424 |
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SourceSKILL.md
| 228 | - [Rehm et al. (2013)](https://pubmed.ncbi.nlm.nih.gov/23887774/) — ACMG clinical laboratory standards for next-generation sequencing. *Genet Med* 15:733–747 |
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SourceSKILL.md
| 229 | - [Miller et al. (2023)](https://pmc.ncbi.nlm.nih.gov/articles/PMC10524344/) — ACMG SF v3.2 list for reporting of secondary findings. *Genet Med* 25:100866 |
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SourceSKILL.md
| 230 | - [Abou Tayoun et al. (2018)](https://pubmed.ncbi.nlm.nih.gov/30192042/) — PVS1 ACMG/AMP variant criterion recommendations. *Human Mutation* 39:1517–1524 |
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SourceSKILL.md
| 231 | - [Li & Wang (2017)](https://pubmed.ncbi.nlm.nih.gov/28132688/) — InterVar: clinical interpretation of genetic variants. *Am J Hum Genet* 100:267–280 |
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SourceSKILL.md
| 232 | - [ClinVar](https://www.ncbi.nlm.nih.gov/clinvar/) — NCBI clinical significance database |
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SourceSKILL.md
| 233 | - [gnomAD](https://gnomad.broadinstitute.org/) — Genome Aggregation Database |
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SourceSKILL.md
| 234 | - [ClinGen](https://clinicalgenome.org/) — Clinical Genome Resource |
Scanned on Jun 11, 2026
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Categoryhealthcare
UpdatedJune 13, 2026
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