41/100 (Medium)

OpenClaw： suspicious
VirusTotal： suspicious
StaticScan： unknown

OpenClaw： suspicious

The skill largely matches its stated purpose (querying ClinVar/dbSNP and producing ACMG-based annotations) but the README claims additional data sources and prediction tools (gnomAD, SIFT/PolyPhen/CAD...

[内容已截断]

VirusTotal： suspicious VT 报告

静态扫描： unknown

README 未提供

{
    "latestVersion": {
        "_creationTime": 1772265678991,
        "_id": "k978kfadk0n4ynhx9z4ddppx19820ffs",
        "changelog": "Initial release of the variant-annotation skill for clinical variant interpretation.\n\n- Query and annotate variants using ClinVar, dbSNP, and population frequency data.\n- Supports multiple input formats: rsID, HGVS notation, genomic coordinates, VCF.\n- Provides clinical significance, ACMG guideline-based classification, allele frequencies, disease associations, and functional predictions.\n- Python API and CLI interfaces for individual and batch variant annotation.\n- Implements ACMG scoring and variant classification thresholds.\n- Integrates major datastores (ClinVar, dbSNP, gnomAD, Ensembl VEP, CADD) for comprehensive annotation.",
        "changelogSource": "user",
        "createdAt": 1772265678991,
        "parsed": {
            "clawdis": {
                "author": "AIPOCH"
            }
        },
        "version": "1.0.0"
    },
    "owner": {
        "_creationTime": 0,
        "_id": "publishers:missing",
        "displayName": "AIpoch",
        "handle": "aipoch-ai",
        "image": "https:\/\/avatars.githubusercontent.com\/u\/258999481?v=4",
        "kind": "user",
        "linkedUserId": "kn76fcc8jhxekae91m2ekbrsgn821avs"
    },
    "ownerHandle": "aipoch-ai",
    "skill": {
        "_creationTime": 1772265678991,
        "_id": "kd7bzq696xt7k2t6bdcme6v47d820sxh",
        "badges": [],
        "createdAt": 1772265678991,
        "displayName": "Variant Annotation",
        "latestVersionId": "k978kfadk0n4ynhx9z4ddppx19820ffs",
        "ownerUserId": "kn76fcc8jhxekae91m2ekbrsgn821avs",
        "slug": "variant-annotation",
        "stats": {
            "comments": 0,
            "downloads": 255,
            "installsAllTime": 1,
            "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": {
            "Gene": "k978kfadk0n4ynhx9z4ddppx19820ffs",
            "Variant": "k978kfadk0n4ynhx9z4ddppx19820ffs",
            "latest": "k978kfadk0n4ynhx9z4ddppx19820ffs"
        },
        "updatedAt": 1774327787026
    }
}