審計歷史
clinvar-database - 4 審計
審計版本 4
最新 低風險Jan 17, 2026, 06:28 AM
This is a documentation-only skill containing markdown files with examples for accessing NCBI's ClinVar database. All 241 static findings are FALSE POSITIVES triggered by code examples in documentation. The skill contains no executable code - only markdown documentation showing legitimate examples for querying a public genomic database. No actual security risks present.
風險因素
審計版本 3
低風險Jan 17, 2026, 06:28 AM
This is a documentation-only skill containing markdown files with examples for accessing NCBI's ClinVar database. All 241 static findings are FALSE POSITIVES triggered by code examples in documentation. The skill contains no executable code - only markdown documentation showing legitimate examples for querying a public genomic database. No actual security risks present.
風險因素
審計版本 2
低風險Jan 12, 2026, 04:57 PM
This is a legitimate documentation skill for accessing NCBI's ClinVar database. The static analysis flagged many false positives from code examples showing curl/wget commands and FTP URLs. These are standard examples for accessing public genomic databases, not security risks.
風險因素
審計版本 1
低風險Jan 4, 2026, 05:00 PM
Documentation-only skill providing ClinVar query guidance. Contains example commands for NCBI API access which is legitimate bioinformatics practice. No executable code or data collection.