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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

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

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

Notes