Pharmgx Reporter
PassAudited by ClawScan on May 1, 2026.
Overview
The skill appears to be a local, user-directed pharmacogenomic report generator; no hidden network, credential, or destructive behavior is evidenced, but it handles sensitive genetic and medication-related information.
Before installing or using this skill, be aware that raw DTC genetic files and the generated pharmacogenomic report are highly sensitive. Use it locally on files you choose, keep the report private, and consult a healthcare professional before making any medication decisions.
Findings (2)
Artifact-based informational review of SKILL.md, metadata, install specs, static scan signals, and capability signals. ClawScan does not execute the skill or run runtime probes.
Using the skill means allowing the included local script to read the chosen genetic file and write a report.
The skill is meant to be run as a local Python script; this is disclosed, user-directed, and central to generating the report.
python pharmgx_reporter.py --input patient_data.txt --output report
Run it only on files you intentionally select, and choose an output directory where you are comfortable storing sensitive health-related results.
If the report is shared, synced, or reused in another context, it may reveal private genetic and medication-related information.
The generated report persistently stores derived genetic variants, phenotypes, and medication-response information, which is sensitive even though this is purpose-aligned.
**Input**: `demo_patient.txt` ... **Genes profiled**: 12 ... ## Detected Variants ... | rsID | Gene | Star Allele | Genotype | Effect |
Keep both the raw genetic file and generated report private, avoid uploading them to shared workspaces unless intended, and delete reports that are no longer needed.