scientific-skills/database-lookup/references/gnomad.md
gnomAD aggregates exome and genome sequencing data to provide allele frequencies and variant annotations across diverse populations.
https://gnomad.broadinstitute.org/apidata wrapper with GraphQL structure)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 } } }"
}
{
"query": "{ gene(gene_symbol: \"BRCA1\", reference_genome: GRCh38) { gene_id symbol chrom start stop strand } }"
}
{
"query": "{ gene(gene_symbol: \"PCSK9\", reference_genome: GRCh38) { variants(dataset: gnomad_r4) { variant_id consequence rsids exome { ac an af } genome { ac an af } } } }"
}
{
"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 } } } }"
}
{
"query": "{ transcript(transcript_id: \"ENST00000357654\", reference_genome: GRCh38) { transcript_id gene_id chrom start stop strand } }"
}
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)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.
{
"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 }
}
}
}
structural_variant)gnomad_constraint