65/100 (Medium)

OpenClaw： suspicious
VirusTotal： benign
StaticScan： clean

OpenClaw： suspicious

The skill's stated purpose (annotating variants using ClinVar/dbSNP and producing ACMG-backed reports) matches the code's use of NCBI E-utilities, but there are coherence issues — the SKILL.md promise...

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VirusTotal： benign VT 报告

静态扫描： clean

No suspicious patterns detected.

README 未提供

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    "latestVersion": {
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        "_id": "k973q36553s1vex4pwyj3vmr1182takh",
        "changelog": "Initial public release of variant-annotation skill.\n\n- Query and annotate gene variants using ClinVar and dbSNP databases, supporting inputs such as rsID, HGVS notation, and genomic coordinates.\n- Provides clinical significance (including ACMG guideline-based classification), allele frequencies, disease associations, and functional predictions.\n- Supports multiple input formats and batch annotation via CLI or Python API.\n- Includes detailed ACMG scoring system for pathogenicity assessment.\n- Integrates data from ClinVar, dbSNP, gnomAD, Ensembl VEP, and CADD.\n- For research\/educational use only; not for clinical diagnostic purposes.",
        "changelogSource": "auto",
        "createdAt": 1773394569768,
        "parsed": {
            "clawdis": {
                "author": "AIPOCH"
            }
        },
        "version": "0.1.0"
    },
    "owner": {
        "_creationTime": 0,
        "_id": "publishers:missing",
        "displayName": "EC-cyber258",
        "handle": "ec-cyber258",
        "image": "https:\/\/avatars.githubusercontent.com\/u\/229709544?v=4",
        "kind": "user",
        "linkedUserId": "kn76a57z1r2t5hjtjfvqaneyf182tqz1"
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    "ownerHandle": "ec-cyber258",
    "skill": {
        "_creationTime": 1773394569768,
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        "badges": [],
        "canonicalSkillId": "kd7bzq696xt7k2t6bdcme6v47d820sxh",
        "createdAt": 1773394569768,
        "displayName": "Variant Annotation",
        "forkOf": {
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            "kind": "duplicate",
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        "latestVersionId": "k973q36553s1vex4pwyj3vmr1182takh",
        "ownerUserId": "kn76a57z1r2t5hjtjfvqaneyf182tqz1",
        "slug": "variant-annotation-2",
        "stats": {
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            "downloads": 111,
            "installsAllTime": 0,
            "installsCurrent": 0,
            "stars": 0,
            "versions": 1
        },
        "summary": "Query and annotate gene variants from ClinVar and dbSNP databases. Trigger when: - User provides a variant identifier (rsID, HGVS notation, genomic coordinat...",
        "tags": {
            "latest": "k973q36553s1vex4pwyj3vmr1182takh"
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        "updatedAt": 1774333007297
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