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Welcome to gnomAD! :wave:
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0
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1049
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June 27, 2023
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PRKCE variant 2-46001442 - G-A (GRCh38)
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4
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64
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December 16, 2025
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Extremely High pLoF Frequency and Homozygote Counts in PRKAG2 (gnomAD v4.1.0)
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0
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5
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December 16, 2025
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4.1 CNV site count on gnomAD website differ from VCF/BED files
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1
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25
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December 9, 2025
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HGDP + 1KG sample metadata discrepency
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0
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27
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December 2, 2025
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Genotype quality for SV call in v4
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1
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47
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November 26, 2025
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Very low allele frequencies in chrX of gnomad4.1 Joint
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1
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18
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November 21, 2025
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Mutation rate table
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1
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74
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November 21, 2025
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Af-only-gnomad.hg38.vcf.gz gnomAD v4/v4.1?
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0
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28
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November 21, 2025
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Urgent query-Genotype Quality for SVs in gnomAD v4.1.0
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3
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39
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November 20, 2025
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Clarification on gnomAD v4.1 Data in GCP
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1
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20
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November 19, 2025
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Gene Deletions as LOF?
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2
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8
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November 19, 2025
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pLOF aggregate frequency data
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0
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8
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November 19, 2025
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LD in release v5
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1
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33
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November 7, 2025
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Conflict in age-related INFO fields
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1
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27
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November 7, 2025
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How to get genome ancestry group data statistics from api
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0
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37
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October 27, 2025
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Grpmax Filtering AF field in v2 vcf files
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1
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31
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September 19, 2025
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gnomAD v5 and All of Us
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1
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125
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September 15, 2025
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Access to Sample-wise Stop-Gain PTV Statistics in ExAC
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0
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29
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September 15, 2025
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SV breakpoints -- are they grouped? How are they determined?
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2
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298
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September 14, 2025
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AC in diseased cohorts (IBD)
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1
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29
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September 12, 2025
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Genome/exome flags in gnomAD v4.1, from the VCF filter field
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2
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51
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September 12, 2025
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gnomAD coverage data and UK BioBank individuals
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1
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32
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September 12, 2025
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Grpmax faf value in gnomAD VCF files
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2
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73
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September 10, 2025
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gnomAD 4.1 non-ukb download?
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2
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73
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September 8, 2025
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GnomAD SVs v4 - discrepancy between hemizygote & male (XY) counts
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14
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354
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August 22, 2025
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Translation correction needed for ALDOA
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1
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60
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August 19, 2025
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How can I tell if two variants occur within an individual?
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1
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63
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August 19, 2025
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Clarification on a 117-bp deletion variant DEL_CHR11_B8445432
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1
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47
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August 19, 2025
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The positions of two deletions are identical. Why weren’t they merged into a single entry?
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1
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61
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August 19, 2025
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