gnomAD Database

Overview

The Genome Aggregation Database (gnomAD) is the largest publicly available collection of human genetic variation, aggregated from large-scale sequencing projects. gnomAD v4 contains exome sequences from 730,947 individuals and genome sequences from 76,215 individuals across diverse ancestries. It provides population allele frequencies, variant consequence annotations, and gene-level constraint metrics that are essential for interpreting the clinical significance of genetic variants.

Key resources:

• gnomAD browser: https://gnomad.broadinstitute.org/
• GraphQL API: https://gnomad.broadinstitute.org/api
• Data downloads: https://gnomad.broadinstitute.org/downloads
• Documentation: https://gnomad.broadinstitute.org/help

When to Use This Skill

Use gnomAD when:

• Variant frequency lookup: Checking if a variant is rare, common, or absent in the general population
• Pathogenicity assessment: Rare variants (MAF < 1%) are candidates for disease causation; gnomAD helps filter benign common variants
• Loss-of-function intolerance: Using pLI and LOEUF scores to assess whether a gene tolerates protein-truncating variants
• Population-stratified frequencies: Comparing allele frequencies across ancestries (African/African American, Admixed American, Ashkenazi Jewish, East Asian, Finnish, Middle Eastern, Non-Finnish European, South Asian)
• ClinVar/ACMG variant classification: gnomAD frequency data feeds into BA1/BS1 evidence codes for variant classification
• Constraint analysis: Identifying genes depleted of missense or loss-of-function variation (z-scores, pLI, LOEUF)

Core Capabilities

1. gnomAD GraphQL API

gnomAD uses a GraphQL API accessible at https://gnomad.broadinstitute.org/api. Most queries fetch variants by gene or specific genomic position.

Datasets available (values of the DatasetId enum):

• gnomad_r4 — gnomAD v4, GRCh38 (recommended default; returns both exome and genome blocks per variant — there is no separate gnomad_r4_genomes id)
• gnomad_r3 — gnomAD v3 genomes, GRCh38
• gnomad_r2_1 — gnomAD v2, GRCh37 (use only for GRCh37 compatibility)

Structural and copy-number variants use separate enums: structural_variants(dataset: gnomad_sv_r4) and copy_number_variants(dataset: gnomad_cnv_r4).

Reference genomes:

• GRCh38 — default for v3/v4
• GRCh37 — for v2

2. Querying Variants by Gene

import requests

def query_gnomad_gene(gene_symbol, dataset="gnomad_r4", reference_genome="GRCh38"):
    """Fetch variants in a gene from gnomAD."""
    url = "https://gnomad.broadinstitute.org/api"

    query = """
    query GeneVariants($gene_symbol: String!, $dataset: DatasetId!, $reference_genome: ReferenceGenomeId!) {
      gene(gene_symbol: $gene_symbol, reference_genome: $reference_genome) {
        gene_id
        symbol
        variants(dataset: $dataset) {
          variant_id
          pos
          ref
          alt
          consequence
          genome {
            af
            ac
            an
            ac_hom
            populations {
              id
              ac
              an
              ac_hom
            }
          }
          exome {
            af
            ac
            an
            ac_hom
          }
          lof
          lof_flags
          lof_filter
        }
      }
    }
    """

    variables = {
        "gene_symbol": gene_symbol,
        "dataset": dataset,
        "reference_genome": reference_genome
    }

    response = requests.post(url, json={"query": query, "variables": variables})
    return response.json()

# Example
result = query_gnomad_gene("BRCA1")
gene_data = result["data"]["gene"]
variants = gene_data["variants"]

# Filter to rare protein-truncating variants.
# Note the parentheses: without them `and` binds tighter than `or`, so the AF
# filter would silently apply only to the consequence branch.
# Per-population frequency is af = ac / an (the populations entries expose
# ac/an, not af). Genome `af` here is absent for variants seen only in exomes,
# so fall back to exome af.
def variant_af(v):
    g = (v.get("genome") or {}).get("af")
    return g if g is not None else (v.get("exome") or {}).get("af", 1)

rare_ptvs = [
    v for v in variants
    if (v.get("lof") == "HC" or v.get("consequence") in ["stop_gained", "frameshift_variant"])
    and variant_af(v) < 0.001
]
print(f"Found {len(rare_ptvs)} rare PTVs in {gene_data['symbol']}")

3. Querying a Specific Variant

import requests

def query_gnomad_variant(variant_id, dataset="gnomad_r4"):
    """Fetch details for a specific variant (e.g., '1-55516888-G-GA')."""
    url = "https://gnomad.broadinstitute.org/api"

    # On a single variant, consequence/lof are NOT top-level fields — they
    # live under transcript_consequences[] (per transcript). Populations
    # expose ac/an only; compute per-population af = ac / an.
    query = """
    query VariantDetails($variantId: String!, $dataset: DatasetId!) {
      variant(variantId: $variantId, dataset: $dataset) {
        variant_id
        chrom
        pos
        ref
        alt
        rsids
        genome {
          af
          ac
          an
          ac_hom
          populations { id ac an ac_hom }
        }
        exome {
          af
          ac
          an
          ac_hom
          populations { id ac an ac_hom }
        }
        transcript_consequences {
          gene_symbol
          major_consequence
          lof
          lof_flags
          is_canonical
        }
        in_silico_predictors {
          id
          value
          flags
        }
      }
    }
    """

    response = requests.post(
        url,
        json={"query": query, "variables": {"variantId": variant_id, "dataset": dataset}}
    )
    return response.json()

# Example: query a specific variant
result = query_gnomad_variant("17-43094692-G-C")  # BRCA1 missense, rs80357199
variant = result["data"]["variant"]

if variant:
    genome_af = (variant.get("genome") or {}).get("af", "N/A")
    exome_af = (variant.get("exome") or {}).get("af", "N/A")
    # Pick the consequence from the canonical transcript when present.
    tcs = variant.get("transcript_consequences") or []
    canonical = next((t for t in tcs if t.get("is_canonical")), tcs[0] if tcs else {})
    print(f"Variant: {variant['variant_id']}")
    print(f"  Consequence: {canonical.get('major_consequence')}")
    print(f"  Genome AF: {genome_af}")
    print(f"  Exome AF: {exome_af}")
    print(f"  LoF: {canonical.get('lof')}")

4. Gene Constraint Scores

gnomAD constraint scores assess how tolerant a gene is to variation relative to expectation:

import requests

def query_gnomad_constraint(gene_symbol, reference_genome="GRCh38"):
    """Fetch constraint scores for a gene."""
    url = "https://gnomad.broadinstitute.org/api"

    query = """
    query GeneConstraint($gene_symbol: String!, $reference_genome: ReferenceGenomeId!) {
      gene(gene_symbol: $gene_symbol, reference_genome: $reference_genome) {
        gene_id
        symbol
        gnomad_constraint {
          exp_lof
          exp_mis
          exp_syn
          obs_lof
          obs_mis
          obs_syn
          oe_lof
          oe_mis
          oe_syn
          oe_lof_lower
          oe_lof_upper
          lof_z
          mis_z
          syn_z
          pLI
        }
      }
    }
    """

    response = requests.post(
        url,
        json={"query": query, "variables": {"gene_symbol": gene_symbol, "reference_genome": reference_genome}}
    )
    return response.json()

# Example
result = query_gnomad_constraint("KCNQ2")
gene = result["data"]["gene"]
constraint = gene["gnomad_constraint"]

print(f"Gene: {gene['symbol']}")
print(f"  pLI:   {constraint['pLI']:.3f}  (>0.9 = LoF intolerant)")
print(f"  LOEUF: {constraint['oe_lof_upper']:.3f}  (<0.35 = highly constrained)")
print(f"  Obs/Exp LoF: {constraint['oe_lof']:.3f}")
print(f"  Missense Z:  {constraint['mis_z']:.3f}")

Constraint score interpretation:

5. Population Frequency Analysis

import requests
import pandas as pd

def get_population_frequencies(variant_id, dataset="gnomad_r4"):
    """Extract per-population allele frequencies for a variant."""
    url = "https://gnomad.broadinstitute.org/api"

    query = """
    query PopFreqs($variantId: String!, $dataset: DatasetId!) {
      variant(variantId: $variantId, dataset: $dataset) {
        variant_id
        genome {
          populations {
            id
            ac
            an
            ac_hom
          }
        }
      }
    }
    """

    response = requests.post(
        url,
        json={"query": query, "variables": {"variantId": variant_id, "dataset": dataset}}
    )
    data = response.json()
    populations = data["data"]["variant"]["genome"]["populations"]

    df = pd.DataFrame(populations)
    df = df[df["an"] > 0].copy()
    df["af"] = df["ac"] / df["an"]
    df = df.sort_values("af", ascending=False)
    return df

# Population IDs in gnomAD v4:
# afr = African/African American
# ami = Amish
# amr = Admixed American
# asj = Ashkenazi Jewish
# eas = East Asian
# fin = Finnish
# mid = Middle Eastern
# nfe = Non-Finnish European
# sas = South Asian
# remaining = Other

6. Structural Variants (gnomAD-SV)

gnomAD also contains a structural variant dataset:

import requests

def query_gnomad_sv(gene_symbol):
    """Query structural variants overlapping a gene."""
    url = "https://gnomad.broadinstitute.org/api"

    # structural_variants requires a dataset argument (gnomad_sv_r4).
    query = """
    query SVsByGene($gene_symbol: String!, $dataset: StructuralVariantDatasetId!) {
      gene(gene_symbol: $gene_symbol, reference_genome: GRCh38) {
        structural_variants(dataset: $dataset) {
          variant_id
          type
          chrom
          pos
          end
          af
          ac
          an
        }
      }
    }
    """

    response = requests.post(
        url,
        json={"query": query, "variables": {"gene_symbol": gene_symbol, "dataset": "gnomad_sv_r4"}}
    )
    return response.json()

Query Workflows

Workflow 1: Variant Pathogenicity Assessment

1. Check population frequency — Is the variant rare enough to be pathogenic?

• Use gnomAD AF < 1% for recessive, < 0.1% for dominant conditions
• Check ancestry-specific frequencies (a variant rare overall may be common in one population)

1. Assess functional impact — LoF variants have highest prior probability

• Check lof field: HC = high-confidence LoF, LC = low-confidence
• Check lof_flags for issues like "NAGNAG_SITE", "PHYLOCSF_WEAK"

1. Apply ACMG criteria:

• BA1: AF > 5% → Benign Stand-Alone
• BS1: AF > disease prevalence threshold → Benign Supporting
• PM2: Absent or very rare in gnomAD → Pathogenic Moderate

Workflow 2: Gene Prioritization in Rare Disease

1. Query constraint scores for candidate genes
2. Filter for pLI > 0.9 (haploinsufficient) or LOEUF < 0.35
3. Cross-reference with observed LoF variants in the gene
4. Integrate with ClinVar and disease databases

Workflow 3: Population Genetics Research

1. Identify variant of interest from GWAS or clinical data
2. Query per-population frequencies
3. Compare frequency differences across ancestries
4. Test for enrichment in specific founder populations

Best Practices

• Use gnomAD v4 (gnomad_r4) for the most current data; use v2 (gnomad_r2_1) only for GRCh37 compatibility
• Handle null responses: Variants not observed in gnomAD are not necessarily pathogenic — absence is informative
• Distinguish exome vs. genome data: Genome data has more uniform coverage; exome data is larger but may have coverage gaps
• Rate limit GraphQL queries: Add delays between requests; batch queries when possible
• Homozygous counts (ac_hom) are relevant for recessive disease analysis
• LOEUF is preferred over pLI for gene constraint (less sensitive to sample size)

Data Access

• Browser: https://gnomad.broadinstitute.org/ — interactive variant and gene browsing
• GraphQL API: https://gnomad.broadinstitute.org/api — programmatic access
• Downloads: https://gnomad.broadinstitute.org/downloads — VCF, Hail tables, constraint tables
• Google Cloud: gs://gcp-public-data--gnomad/

Additional Resources

• gnomAD website: https://gnomad.broadinstitute.org/
• gnomAD blog: https://gnomad.broadinstitute.org/news
• Downloads: https://gnomad.broadinstitute.org/downloads
• API explorer: https://gnomad.broadinstitute.org/api (interactive GraphiQL)
• Constraint documentation: https://gnomad.broadinstitute.org/help/constraint
• Citation: Karczewski KJ et al. (2020) Nature. PMID: 32461654; Chen S et al. (2024) Nature. PMID: 38057664
• GitHub: https://github.com/broadinstitute/gnomad-browser

Scripts

scripts/query_gnomad.py — runnable helper for the gnomAD GraphQL API (no key). It carries inline PEP 723 deps, so run the file directly with uv run (not uv run python ...) to auto-install requests:

uv run scripts/query_gnomad.py variant 17-43094692-G-C --dataset gnomad_r4
uv run scripts/query_gnomad.py constraint BRCA1 --genome GRCh38