myvariant.variants.batch
Retrieve annotations for up to 1000 genetic variants in a single request by providing a comma-separated list of dbSNP rsIDs or HGVS variant IDs. Returns ClinVar significance, CADD scores, gnomAD allele frequencies, and functional consequence predictions for each variant in one call. Ideal for ann...
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What myvariant.variants.batch does on Apibase
AI agents call myvariant.variants.batch to retrieve information from Apibase without modifying anything. It is typically the context-gathering step in research, monitoring, and reporting workflows, before the agent takes action elsewhere.
| Parameter | Type | Required | Description |
|---|---|---|---|
ids | string | Yes | Comma-separated list of variant identifiers to retrieve in a single request. Accepts dbSNP rsIDs (e.g. "rs58991260,rs671,rs1801133") or HGVS genomic IDs. Mix of |
fields | string | — | Comma-separated annotation fields to return for each variant. Default: dbsnp,clinvar,cadd,gnomad_exome,gnomad_genome,snpeff,vcf,chrom,hg19. Limit fields for lar |
Parameters from the server's own tool schema.
Why myvariant.variants.batch is rated Low
Retrieves and queries genetic variant annotations without modifying data or triggering external operations.
From the tool's definition Retrieve annotations for genetic variants, Returns ClinVar significance, CADD scores, gnomAD allele frequencies
Attacks that exploit this kind of access
The rule that runs myvariant.variants.batch safely
PolicyLayer is an MCP gateway: it sits between your AI agents and Apibase, and checks every tool call against a rule you set before the call runs. Nothing changes on the server itself. For myvariant.variants.batch, this is the rule to start with:
myvariant.variants.batch is read-only, so it stays allowed. Everything else on the server is denied unless you say otherwise.
The button opens the PolicyLayer dashboard: create your workspace, connect Apibase, apply this rule, and every myvariant.variants.batch call is checked against it from then on.
Questions about myvariant.variants.batch
Retrieve annotations for up to 1000 genetic variants in a single request by providing a comma-separated list of dbSNP rsIDs or HGVS variant IDs. Returns ClinVar significance, CADD scores, gnomAD allele frequencies, and functional consequence predictions for each variant in one call. Ideal for annotating VCF files, enriching GWAS hit lists, building polygenic risk score pipelines, or bulk pharmacogenomics analysis. Variants not found in the database are marked with found=false. Mix rsIDs from different chromosomes freely — no grouping by position required. It is categorised as a Read tool in the Apibase MCP Server, which means it retrieves data without modifying state.
myvariant.variants.batch accepts 2 parameters: ids, fields. Required: ids. The full parameter table on this page comes from the server's own tool schema.
Register the Apibase MCP server in PolicyLayer and add a rule for myvariant.variants.batch: allow, deny, rate-limit, or require approval. Point your MCP client at the PolicyLayer proxy URL and the rule is enforced on every call, before it reaches Apibase. Nothing to install.
myvariant.variants.batch is a Read tool with low risk. Read-only tools are generally safe to allow by default.
Yes. Add a rate_limit block to the myvariant.variants.batch rule in your PolicyLayer policy. For example, setting max: 10 and window: 60 limits the tool to 10 calls per minute. Rate limits are tracked per agent session and reset automatically.
Set action: deny in the PolicyLayer policy for myvariant.variants.batch. The AI agent will receive a policy violation error and cannot call the tool. You can also include a reason field to explain why the tool is blocked.
myvariant.variants.batch is provided by the Apibase MCP server (apibase-mcp-client). PolicyLayer sits as a proxy in front of this server to enforce policies before tool calls reach the server.
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