Folklore Variant Evidence

Resolve and classify one public GRCh38 germline variant with Folklore. Accepts coordinates, genomic, coding and protein HGVS, SPDI and rsID; returns normalized identity, ACMG/AMP decision support, evidence, provenance and limitations for professional review.

该来源不提供完整文件导出（国内平台多为平台内托管），仅存元数据与原链

模型生成摘要（rules/v1 · 2026-09-27 16:51）：Resolve and classify one public GRCh38 germline variant with Folklore
这是模型对公开材料的总结，不是官方声明，请以原链内容为准。

接入信息

传输形态: http
鉴权方式: 鉴权未知
端点: https://folklore--helena-bioinformatics.run.tools

鉴权方式未标注，请核对官方文档后再接入——不要直接使用以下片段

{
  "mcpServers": {
    "Folklore Variant Evidence": {
      "url": "https://folklore--helena-bioinformatics.run.tools"
    }
  }
}

能力清单

工具

说明

search_variant_evidence

Classify, interpret or resolve one public GRCh38 germline SNV or simple indel smaller than 50 bp. Accepts coordinates, genomic/coding/protein HGVS, SPDI or rsID. Returns normalized variant identity, automated ACMG/AMP decision support, evidence, provenance and explicit limitations. This is variant-level decision support for professional review. It does not evaluate patient context and must not be presented as a diagnosis or treatment recommendation. Never choose a candidate when resolution is ambiguous.

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