search_variant_evidence
shallowio.github.helena-bioinformatics/folklore · Verify this server
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.
No longer in the registry. The MCP registry stopped listing this server as of 11 Sept 2026. This report card stays available because the measurement was real, but the tool is excluded from search, rankings, and Vouch’s corpus counts. A published behaviour score is never recomputed or removed — it reflects what was measured while the server was listed.
2 trials · measured 55 days ago
search_variant_evidence scores 100.0/100 on Vouch's measured behaviour index, from 2 real invocation trials against io.github.helena-bioinformatics/folklore, measured 25 Aug 2026 under methodology v0.2.0. Every measured component scored 100.
Component breakdown
| Component | Weight | Value |
|---|---|---|
| Reliability | 35% | not applicable |
| Schema integrity | 25% | 100.0 |
| Failure behaviour | 15% | not applicable |
| Latency | 15% | not applicable |
| Concurrency | 10% | not applicable |
Tool details
- Transport
- remote
- Credential class
- unreachable
- Category
- Health
- Input schema
- not declared
- Output schema
- not declared
- Side-effect classification
- read-only— Heuristically read-only-eligible (readonly-heuristic.ts) and sample-called by the Phase 0 census shallow probe.
Score history
| Day | Score | Tier | Methodology |
|---|---|---|---|
| 2026-08-25 | 100.0 | shallow | v0.2.0 |
Probe evidence
| Probe | Outcomes |
|---|---|
| schema_integrity | pass: 1 |
| sample_call | pass: 1 |
Raw request/response logs are not archived yet — the outcome counts above are drawn directly from every recorded trial.
Embed this score
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