gnomad-genetics-mcp-server
One of the ways to connect Gnomad Genetics
Look up variant allele frequencies by ancestry, gene loss-of-function constraint, gene variant lists, and sequencing coverage over gnomAD — with ClinVar significance joined in — via MCP. STDIO or Streamable HTTP.
Provides ancestry allele frequencies, LoF constraint, variant lists, and coverage from gnomAD, joined with ClinVar clinical significance. Supports querying large result sets with SQL.
- Version:
- 0.5.2
- Publisher:
- cyanheads
- Company:
- Cyanheads (third-party)
- Summary written by google/gemini-2.5-flash-lite from the server’s own site and README; facts above come from the registries.
- Logo: https://cursor.com/deeplink/mcp-install-dark.svg
Install
Generated from the server’s transport data — never hand-written. Placeholders in angle brackets are yours to fill.
Run it with its own identity, a budget you set, and every call audited — no local config to keep in sync.
Add to a connect0 projectYou will sign in first, then land back on this page.
What it can do
No capability summary yet — the publisher has not declared one and it has not been verified.