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gnomAD (Genome Aggregation Database) API Reference
``` POST https://gnomad.broadinstitute.org/api Content-Type: application/json
Claude Code Knowledge Pack7/10/2026
Overview
gnomAD (Genome Aggregation Database) API Reference
Overview
gnomAD aggregates exome and genome sequencing data to provide allele frequencies and variant annotations across diverse populations.
API Type: GraphQL
- Endpoint:
https://gnomad.broadinstitute.org/api - Method: POST with JSON body containing GraphQL query
- Auth: None required (public, unauthenticated)
- Response format: JSON (
datawrapper with GraphQL structure)
Key Queries
Variant lookup by variant ID
Variant IDs use format: {chrom}-{pos}-{ref}-{alt} (GRCh37 or GRCh38).
POST https://gnomad.broadinstitute.org/api
Content-Type: application/json
{
"query": "{ variant(variantId: \\"1-55516888-G-A\\", dataset: gnomad_r4) { variant_id rsids chrom pos ref alt exome { ac an af } genome { ac an af } } }"
}
Gene lookup
{
"query": "{ gene(gene_symbol: \\"BRCA1\\", reference_genome: GRCh38) { gene_id symbol chrom start stop strand } }"
}
Variants in a gene
{
"query": "{ gene(gene_symbol: \\"PCSK9\\", reference_genome: GRCh38) { variants(dataset: gnomad_r4) { variant_id consequence rsids exome { ac an af } genome { ac an af } } } }"
}
Variants in a region
{
"query": "{ region(chrom: \\"1\\", start: 55505222, stop: 55530526, reference_genome: GRCh38) { variants(dataset: gnomad_r4) { variant_id rsids consequence exome { ac af } genome { ac af } } } }"
}
Transcript lookup
{
"query": "{ transcript(transcript_id: \\"ENST00000357654\\", reference_genome: GRCh38) { transcript_id gene_id chrom start stop strand } }"
}
Dataset values
gnomad_r4-- gnomAD v4 (GRCh38, latest major release)gnomad_r3-- gnomAD v3.1.2 (GRCh38, genomes only)gnomad_r2_1-- gnomAD v2.1.1 (GRCh37, exomes + genomes)
Population frequency fields
Within exome or genome objects, population-specific frequencies are available via
populations { id ac an af } where id values include: afr, amr, asj, eas,
fin, mid, nfe, oth, sas.
Response example (variant)
{
"data": {
"variant": {
"variant_id": "1-55516888-G-A",
"rsids": ["rs11591147"],
"chrom": "1",
"pos": 55516888,
"ref": "G",
"alt": "A",
"exome": { "ac": 1234, "an": 250000, "af": 0.004936 },
"genome": { "ac": 456, "an": 150000, "af": 0.00304 }
}
}
}
Rate Limits
- No published rate limits, but aggressive querying will be throttled
- Use reasonable request pacing (~1 req/sec recommended)
- For bulk downloads, use gnomAD's Hail tables on Google Cloud or download VCFs
Notes
- The GraphQL schema is not versioned separately; it tracks the gnomAD web interface
- Use the browser's network inspector on gnomad.broadinstitute.org to discover additional query fields and structures
- Structural variants (SV) have a separate query structure (
structural_variant) - Constraint metrics (pLI, LOEUF) are available on gene queries via
gnomad_constraint