sniff-mcp (Sniffscore/sniff-mcp) is an MCP server listed on the M8ven Trust Index. It scores 43 out of 100, grade D. It declares 17 tools. No publisher has claimed this listing.
Agent-callable canine genomics API providing breed-stratified allele frequencies, pathogenicity predictions, and variant-gene-breed-disease knowledge graph for dog DNA.
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The grade above is for the source repository. Registries can serve a different version, so we mark the ones we were not able to read.
These names and descriptions are the publisher's own, read from the source code. We print them as written. Our assessment is the findings above, not this list.
askAsk Sniff a natural-language canine-genetics question and get a GROUNDED, CITED answer (or an honest abstain). Covers inherited diseases (OMIA) and their human homologs (the dog<->human disease bridge), breed disease/carrier risk, variant pathogenicity grades (AVCG; Boeykens et al. 2024, curated in …
disease_bridgeThe fused OMIA disease layer as cited atoms. Give a `disease` (name or 'OMIA:001870-9615') for its genes, inheritance, human homolog (OMIM/Mondo bridge), and variant pathogenicity grade (AVCG, ACMG/AMP 5-tier, curated in OMIA) when graded. Or give a `breed` (e.g. 'doberman_pinscher') for the inherit…
ask_variant_contextTHE headline query. Given a CanFam4 position (e.g. '5:56189113'), return the variant's global + popmax frequency, breed-stratified cross-breed frequencies, ESM2/Pangolin/phyloP pathogenicity, gene context, linked diseases (v1.1), provenance, and deep links — in one call. Pass breed_context to also g…
variant_lookupSingle-variant lookup by CanFam4 position: ref/alt, global + popmax AF, consequence, gene, ESM2/Pangolin/phyloP, deleteriousness tier, canonical URL, provenance.
breed_variant_frequencyBreed-stratified allele frequency. Give a breed (e.g. 'bernese_mountain_dog') plus either a variant position or a gene symbol. Returns AF (+ rank) for the variant, or per-variant AFs in the gene.
gene_summaryVariants in a gene (by gene symbol), ranked by impact then ESM2 damage. Paginated (limit, default 25); returns total_variants. Use af_min to filter by global AF.
breed_summaryBreed profile: top damaging common variants (ESM2<=-5 & breed AF>=5%), n_dogs, breed group. Descriptive only — not a health ranking.
variant_searchFiltered discovery over all 9.67M variants. Predicates (combine freely): esm_max (ESM2 LLR <=), phylop_min (phyloP >=), popmax_min (popmax AF >=), gene_in (list of gene symbols), consequence, impact (HIGH/MODERATE/LOW/MODIFIER). Returns total_count + a capped list (max 200). Note: popmax may be in a…
nearest_breedsGenetically nearest breeds to the given breed (top-10-PC Euclidean in canine genetic space). Answers 'what breeds are most genetically similar to X?' via the PCA-256 breed co-embedding.
breed_similarityGenetic distance between two breeds (top-10-PC Euclidean). Lower = more genetically similar.
semantic_searchFaceted hybrid + semantic-ranker search over the whole knowledge base (diseases, breeds, Scout discoveries). Use for fuzzy/thematic intent ('drug sensitivity in herding dogs', 'breeds prone to eye disease', 'genetically diverse breeds'). entity_type filters to 'disease'|'breed'|'discovery'. filters …
disease_linksA canine inherited disease (name or OMIA id) -> its governed OMIA clinical record: mode of inheritance, causal gene(s), curated description (summary / clinical features / molecular genetics / pathology / prevalence), clinical signs as HP/MP phenotype terms (-> Monarch), the human OMIM analog + Mondo…
disease_lookupLook up a canine inherited disease by name or OMIA id -> its governed OMIA clinical record (inheritance, causal gene(s), curated description, clinical signs, human OMIM analog + Mondo id, evidence base). Sourced to OMIA (CC-BY); returns a canonical sniff.world URL. Dog-only. For candidate disambigua…
search_diseasesSearch the canine disease catalogue by free text -> ranked candidates [{omia_id, disease, url, score}]. Use before disease_lookup when the exact name is unknown. Dog-only.
breeds_in_atlasList all 188 breeds with breed-stratified frequencies in the atlas.
genes_indexedTop genes by number of variants in the atlas (discovery aid).
metadataAtlas metadata: release, DOI, assembly, variant/breed counts, scope banner, and the RPC catalog.
SNIFF_MCP_URLSNIFF_BRAIN_URLSNIFF_BREEDDIMSNIFF_EMBSNIFF_SEARCH_ENDPOINTSNIFF_SEARCH_KEY_FILESNIFF_SEARCH_INDEXSNIFF_KGDIRSNIFF_PLAINSNIFF_DISCOVERIESSNIFF_MASTERSNIFF_BREEDAFSNIFF_STORESNIFF_RELEASESNIFF_OMIA_DIRSNIFF_DATAR2_BUCKETR2_ACCOUNT_IDR2_ACCESS_KEY_IDR2_SECRET_ACCESS_KEYSNIFF_SEARCH_KEYAZURE_OPENAI_ENDPOINTAZURE_OPENAI_KEYSNIFF_EMBED_DEPLOYSNIFF_COMPANION_CTXSNIFF_DOGDIMSNIFF_BREED_NEIGHBORSPORTTool annotations
No tools have read-only/destructive annotations
Add readOnlyHint or destructiveHint annotations to every tool so hosts can warn users before invoking.
All four hints declared on every tool
17/17 tools missing one or more hints — ask (missing: readOnlyHint, destructiveHint, idempotentHint, openWorldHint); disease_bridge (missing: readOnlyHint, destructiveHint, idempotentHint, openWorldHint); ask_variant_context (missing: readOnlyHint, destructiveHint, idempotentHint, openWorldHint), +14 more. OpenAI's directory rejects tools where any of the four hints are missing or non-boolean.
For every tool, set all four hints (readOnlyHint, destructiveHint, idempotentHint, openWorldHint) to explicit true/false values that match the handler’s actual behaviour.
Tests exist
No test files found
Add tests that exercise each declared tool.
No access to sensitive paths
Reads sensitive paths: /home/ubuntu/.sniff_openai.env
Remove reads of sensitive system paths. If you genuinely need them, document why in the README.
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