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The Genome Aggregation Database (gnomAD), produced by the Broad Institute, is a population-scale resource that aggregates and harmonizes exome and genome sequencing data from multiple research projects. It provides aggregated allele frequencies, variant calls, and annotations for human genetic variation across diverse populations. Researchers use gnomAD to filter rare variants, estimate population frequencies, and support interpretation of genetic variants in disease studies.
We haven’t found gnomAD in the AI answers we’ve checked.