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myvariant.variants.info

Retrieve comprehensive annotation for a single genetic variant by its dbSNP rsID (e.g. "rs671") or HGVS genomic notation. Returns complete annotation from 30+ integrated databases: ClinVar clinical significance and disease conditions, CADD pathogenicity scores (raw + PHRED), gnomAD exome and geno...

SERVERApibase SOURCEapibase-mcp-client
Low RISK CLASS
Category Read
Parameters 21 required
Recommended Allowedsee the rule below
Registry record Grade F, identity unverified Pull the record →

This record as markdown: /tools/io-github-whiteknightonhorse-apibase/myvariant.variants.info.md

What myvariant.variants.info does on Apibase

AI agents call myvariant.variants.info 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.

ParameterTypeRequiredDescription
fields string — Comma-separated annotation fields to retrieve. Default: dbsnp,clinvar,cadd,gnomad_exome,gnomad_genome,snpeff,vcf,chrom,hg19. Optional: dbnsfp (functional predic
variant_id string Yes Variant identifier — dbSNP rsID (e.g. "rs58991260"), or HGVS genomic notation (e.g. "chr7:g.140453134A>T" — use URL-encoded form when needed). rsIDs are preferr

Parameters from the server's own tool schema.

Why myvariant.variants.info is rated Low

Tool queries genetic variant databases and returns annotations without modifying data.

From the tool's definition Retrieve comprehensive annotation for a single genetic variant

Questions about myvariant.variants.info

What does the myvariant.variants.info tool do? +

Retrieve comprehensive annotation for a single genetic variant by its dbSNP rsID (e.g. "rs671") or HGVS genomic notation. Returns complete annotation from 30+ integrated databases: ClinVar clinical significance and disease conditions, CADD pathogenicity scores (raw + PHRED), gnomAD exome and genome allele frequencies across ancestry groups (AFR, EUR, EAS, AMR, ASJ), SnpEff predicted functional consequences with HGVS coding and protein notations, dbSNP allele frequency data, COSMIC somatic mutation records, CIViC clinical interpretations, and genomic coordinates in both GRCh37 (hg19) and GRCh38 (hg38). Essential for variant interpretation pipelines, pharmacogenomics analysis, and clinical variant classification (ACMG guidelines). It is categorised as a Read tool in the Apibase MCP Server, which means it retrieves data without modifying state.

What parameters does myvariant.variants.info accept? +

myvariant.variants.info accepts 2 parameters: fields, variant_id. Required: variant_id. The full parameter table on this page comes from the server's own tool schema.

How do I enforce a policy on myvariant.variants.info? +

Register the Apibase MCP server in PolicyLayer and add a rule for myvariant.variants.info: 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.

What risk level is myvariant.variants.info? +

myvariant.variants.info is a Read tool with low risk. Read-only tools are generally safe to allow by default.

Can I rate-limit myvariant.variants.info? +

Yes. Add a rate_limit block to the myvariant.variants.info 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.

How do I block myvariant.variants.info completely? +

Set action: deny in the PolicyLayer policy for myvariant.variants.info. 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.

What MCP server provides myvariant.variants.info? +

myvariant.variants.info 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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