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.
Published
June 28, 2026
6d ago
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License Sources Match
Apache-2.0 confirmed by 2 independent sources — npm registry metadata and the LICENSE file in the package source — as of July 3, 2026.
| Source | License | Class |
|---|---|---|
Licensie (detected) | Apache-2.0 | Permissive |
npm (reported) | Apache-2.0 | Permissive |
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