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songlab/
gnomad-full

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gnomAD v4.1 Variants with Consequence Annotations

This dataset contains SNVs from gnomAD v4.1 genomes joined with variant consequence annotations. Code: https://github.com/gonzalobenegas/gnomad

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	Coordinates

chrom: Chromosome (1-22, X, Y) pos: Position (1-based) ref: Reference allele alt: Alternate allele

gnomAD Allele Frequencies

AC: Allele count AN: Allele number AF: Allele frequency

	Consequence Annotations… See the full description on the dataset page: https://huggingface.co/datasets/songlab/gnomad-full.