← deepdna.ai

INDIVIDUAL MCP TOOL

request_beta_access

Register the user's interest in DeepDNA's private beta (DNA file parsing, annotation, bloodwork; not deployed yet).

deepdna.ainone authenticationAvailability not checked

LIVE ENDPOINT

https://deepdna.ai/mcp

No auth detected

Connect to this endpoint to inspect the live schema for request_beta_access and invoke it with your own arguments.

Indexed input schema

{}

Risk classification

Inferred read-only · medium confidence · heuristic, not a guarantee.

  • No write-capable action terms were found; this is not proof that invocation has no side effects.

Parent server

deepdna.ai

CONNECT WITH APPROVAL

Client installation

Review this server and its permissions before adding it. Secret placeholders must be set locally.

Codex

~/.codex/config.toml

[mcp_servers.deepdna]
url = "https://deepdna.ai/mcp"
enabled = true
Claude Code

.mcp.json

{
  "mcpServers": {
    "deepdna": {
      "type": "http",
      "url": "https://deepdna.ai/mcp"
    }
  }
}
Claude Desktop

Settings → Connectors → Add custom connector

Name: deepdna
Remote MCP URL: https://deepdna.ai/mcp

Add this remote URL as a custom connector in Claude Desktop. Availability depends on the user plan and workspace policy.

Cursor

.cursor/mcp.json

{
  "mcpServers": {
    "deepdna": {
      "url": "https://deepdna.ai/mcp"
    }
  }
}
Visual Studio Code

.vscode/mcp.json

Add to Visual Studio Code
{
  "servers": {
    "deepdna": {
      "type": "http",
      "url": "https://deepdna.ai/mcp"
    }
  }
}
Generic MCP

Client-specific MCP configuration

{
  "name": "deepdna",
  "transport": "streamable-http",
  "url": "https://deepdna.ai/mcp"
}
MCP Inspector

Run the official MCP Inspector locally and enter the indexed Streamable HTTP endpoint.

Related tools

  • list_genes — List the genes in the DeepDNA knowledge base, with a one-line summary and category for each.
  • lookup_gene — Everything curated about one gene: function, key variants with rsIDs, metabolizer or function phenotypes, drug interactions, what a consumer genotyping array can and cannot tell you, and sources.
  • lookup_variant — One variant by dbSNP rsID: gene, star-allele or common name, alleles, functional effect, population frequency and sources.
  • lookup_drug_gene — Pharmacogenomic guidance for a gene, optionally for one drug: guideline (CPIC or DPWG, "drug label", or null when the record rests on the primary literature), summary of the recommendation, phenotypes and sources.
  • check_medications — Given a list of generic drug names, say which ones have a curated drug–gene record, with which genes and what each record rests on (a CPIC or DPWG guideline, a drug label, or the primary literature), and which are not covered.