clarity-clinical

Query clinical variant data from ClinVar and gnomAD via Clarity Protocol. Use when the user asks about ClinVar classification, clinical significance, pathogenicity, gnomAD frequency, population genetics, or clinical data for gene. Capabilities: search clinical variants by gene, get detailed variant annotations.

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Repository: johnalbertini14-glitch/openclaw-skills
Last source activity: February 25, 2026 at 20:31
Detected SKILL.md language: English
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Forks: 0

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name	clarity-clinical
description	Query clinical variant data from ClinVar and gnomAD via Clarity Protocol. Use when the user asks about ClinVar classification, clinical significance, pathogenicity, gnomAD frequency, population genetics, or clinical data for gene. Capabilities: search clinical variants by gene, get detailed variant annotations.
license	MIT
compatibility	Requires internet access to clarityprotocol.io. Optional CLARITY_API_KEY env var for 100 req/min (vs 10 req/min).
metadata	{"author":"clarity-protocol","version":"1.0.0","homepage":"https://clarityprotocol.io"}