genomi-gnomad
GitHub通过 gnomAD 获取特定变体的公共群体等位基因频率,支持 MAF、人群分层计数及罕见度查询。仅针对单变异点,结果本地缓存以复用。适用于需验证特定 rsID 或坐标变体频率的场景,不用于全基因组筛选。
Trigger Scenarios
Install
npx skills add exon-research/genomi --skill genomi-gnomad -g -y
SKILL.md
Frontmatter
{
"name": "genomi-gnomad",
"tools": [
"genomi.invoke"
],
"mutating": true,
"description": "Fetch reusable public population allele frequencies from gnomAD for a\nspecific variant. Use when the user asks about allele frequency, MAF,\npopulation stratification, gnomAD numbers, or rarity of a specific allele.\n"
}
Population Frequency (gnomAD)
Fetch public gnomAD population allele frequencies for one variant. Results are cached locally in the evidence database so subsequent queries reuse them.
Activation
To call the tool below, invoke it through the MCP dispatcher:
genomi.invoke({
"tool": "gnomad.fetch_population_frequency",
"params": {
"chrom": "19",
"pos": 44908684,
"ref": "T",
"alt": "C",
"genome_build": "GRCh38"
}
})
The dispatcher validates the params against the underlying tool's input
schema and returns the underlying tool's response with an added
dispatched_tool field.
When to use this skill
- "What is the gnomAD frequency of rs429358?"
- "Is this variant rare in gnomAD?"
- "Allele frequency in African populations for rs1042522."
- Any question that needs MAF, AF, population-stratified counts.
Boundaries
- Variant-anchored only — query one allele at a time.
- Public population data only — does not read the user's Active Genome Index.
- Cached after first fetch — subsequent queries for the same variant reuse the local evidence store.
Cross-Capability Synthesis
A scope-limited result from this capability is not a final user-facing answer when other Genomi capabilities can contribute orthogonal evidence to the same question. Returning "cannot answer" while applicable capabilities remain unexamined is a host-agent failure mode.
Tools
gnomad.fetch_population_frequency
Fetch reusable gnomAD public population frequency for one allele and write it into evidence storage.
Use when: The agent needs gnomAD allele frequency, MAF, or population-stratified counts for a specific variant (rsID, chrom/pos/ref/alt, or VCF locus).
Why necessary: gnomAD is the canonical public population frequency source; cached results keep subsequent calls cheap.
Not for: Genome-wide rare-variant screening, ad-hoc curated annotations, anything not anchored to a specific variant.
Example prompts: What's the gnomAD frequency of rs429358? Is rs1042522 rare in East Asian populations?
Result semantics: Returns the gnomAD record with population-stratified counts and frequencies plus a populations block; writes to the local evidence database for reuse.
Version History
- 47e0d05 Current 2026-07-05 10:53


