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Welcome to gnomAD! :wave:
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0
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1175
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June 27, 2023
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About the General category
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0
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231
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June 27, 2023
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gnomAD v4.1 cohort inclusion
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1
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51
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August 11, 2026
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Finding SNV's associated with common diseases
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0
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18
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August 7, 2026
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HGDP 1kG call set phasing information
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1
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25
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August 7, 2026
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gnomAD v5 - planned release?
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3
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46
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August 5, 2026
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GroupMax values missing for a lot of variants
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10
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845
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August 4, 2026
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Quantifying not-normal reported variant frequencies
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0
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20
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June 27, 2026
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My Java version is: openjdk version "18" 2022-03-22
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0
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22
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June 7, 2026
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V4.1.1 variant md5sums outdated
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2
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47
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May 27, 2026
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Feedback from using the GraphQL API for ClinPGx
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0
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47
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May 19, 2026
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Stratified coverage counts for gnomAD v4
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1
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42
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May 12, 2026
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Presentation on misconceptions about gnomAD
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0
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58
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May 12, 2026
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Mapping Quality and Pseudogene Interference
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0
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26
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May 8, 2026
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Variant is in gnomAD, not in gnomAD non-UKB, but also not in UKB
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2
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53
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April 28, 2026
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Can someone help with TFRC variant?
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2
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89
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March 12, 2026
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Discrepancies in AN values for multiallelic sites
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2
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80
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February 26, 2026
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Paths to all HGDP and 1KG bam files
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1
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54
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February 23, 2026
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P.met2864ile Variant
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1
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45
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February 20, 2026
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Service overloaded
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4
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101
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February 19, 2026
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SLC2A1 variant information please help!
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1
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56
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February 6, 2026
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Access Tunisian data
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1
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38
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February 5, 2026
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Download files - coverage: v3 has genome cov., Gnomad v4 has only exome cov
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2
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54
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January 29, 2026
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HGDP + 1KG sample metadata discrepency
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2
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105
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January 28, 2026
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Discrepancies in allele frequencies for Admixed American population
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0
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49
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January 27, 2026
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Total Grpmax Filtering AF gnomAD v4.1.0 vs gnomAD v4.1.0 (non-UKB)
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2
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95
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January 15, 2026
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PRKCE variant 2-46001442 - G-A (GRCh38)
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4
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139
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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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42
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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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92
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December 9, 2025
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Very low allele frequencies in chrX of gnomad4.1 Joint
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1
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53
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November 21, 2025
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