gnomad_list_gene_variants

shallow

io.github.cyanheads/gnomad-genetics-mcp-server · Verify this server

List every gnomAD variant in a gene, transcript, or region with allele frequencies and predicted consequences, optionally filtered to one consequence class (lof, missense, synonymous, other) and/or a maximum allele frequency. The full result is staged on a DataCanvas table named gene_variants and an inline preview is returned alongside canvas_id and table_name — run gnomad_dataframe_query against them to rank by AF, count by consequence, or group across the complete set rather than the preview. When the canvas is disabled (CANVAS_PROVIDER_TYPE != duckdb) the tool returns a capped inline preview with spilled=false and canvas_id empty; the SQL path is then unavailable. Supply exactly one of gene, transcript_id, or region. Echoes the effective dataset and build.

100.0/100

1 trials · measured 2 days ago

gnomad_list_gene_variants scores 100.0/100 on Vouch's measured behaviour index, from 1 real invocation trials against io.github.cyanheads/gnomad-genetics-mcp-server, measured 31 Aug 2026 under methodology v0.2.0. Every measured component scored 100.

Component breakdown

ComponentWeightValue
Reliability35%not applicable
Schema integrity25%100.0
Failure behaviour15%not applicable
Latency15%not applicable
Concurrency10%not applicable

Tool details

Transport
remote + stdio
Credential class
self-provisionable
Input schema
not declared
Output schema
not declared
Side-effect classification
unclassified

Score history

DayScoreTierMethodology
2026-08-31100.0shallowv0.2.0

Probe evidence

ProbeOutcomes
schema_integritypass: 1

Raw request/response logs are not archived yet — the outcome counts above are drawn directly from every recorded trial.

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Vouch score: gnomad_list_gene_variants
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gnomad_list_gene_variants — Vouch