allele-registry-mcp-server

Item: allele-registry-mcp-server
Rating: 0
Author: M8ven

Enables resolving genetic variant identifiers (HGVS, dbSNP, ClinVar, gnomAD) to stable ClinGen Allele Registry IDs (CA#) and cross-references, providing a canonical allele identity across genome builds.

→ QuentinCody/allele-registry-mcp-server · listed on glama

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// key findings

🚨

Reads files from sensitive locations

Touches: /../etc/passwd

⚠️

Known vulnerabilities in dependencies: 1 high

Affects packages this MCP installs at runtime. Upgrade or remove the affected dependency.

// known CVEs in dependencies1 high

Disclosed vulnerabilities in this server's declared npm dependencies (via OSV). Whether each is reachable depends on the installed versions.

highwrangler@4.56.0GHSA-36p8-mvp6-cv38

Wrangler affected by OS Command Injection in `wrangler pages deploy`

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// full audit trail

The full breakdown of what we checked, the deductions that landed, the network hosts, the dependency advisories, and concrete fix guidance is available to verified publishers.

// improvement guidance — verified publishers only

We have 5 concrete improvements we can share with the publisher of this MCP. Each comes with specific guidance to raise the trust score.

// embed badge in your README

[![M8ven Score](https://m8ven.ai/badge/mcp/quentincody-allele-registry-mcp-server-12r84q)](https://m8ven.ai/mcp/quentincody-allele-registry-mcp-server-12r84q)

commit: 17d0ba039abfc551a0b7715385077d1531a0231a

code hash: f5fbb0bb599026530c335f9167590154bf3f6230b140956e0780ef7d42dd61d3

verified: 7/11/2026, 8:24:54 AM

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