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Welcome to gnomAD! :wave:
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0
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1220
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June 27, 2023
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BRCA1 gene page fails to load tonight
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3
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48
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September 10, 2026
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Missing Data in your database
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1
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31
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September 9, 2026
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Variant search - HGVS support
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0
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24
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September 9, 2026
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Gnomad WGS AFs are often ~10x the Gnomad WES AF
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0
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51
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September 2, 2026
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MPC v4.1.1 transcript count in paper differs from score file
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0
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37
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August 27, 2026
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Service overloaded
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5
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170
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August 25, 2026
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gnomAD v4.1 cohort inclusion
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1
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97
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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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43
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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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59
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August 7, 2026
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gnomAD v5 - planned release?
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3
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114
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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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910
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August 4, 2026
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Tandem Repeat: PRE-MIR7-2
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2
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114
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August 2, 2026
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Urgent query - discrepancy between SVs v2.1 & SVs v4.1: missing hemizygotes in the larger dataset
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2
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88
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July 6, 2026
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Filtering the v4 Exome CNV VCF
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0
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48
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July 1, 2026
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Missense constraint updated in v4.1.1?
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0
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63
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June 29, 2026
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Quantifying not-normal reported variant frequencies
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0
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35
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June 27, 2026
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Best practices for filtering Manta SV calls before comparison with gnomAD-SV?
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0
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60
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June 9, 2026
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My Java version is: openjdk version "18" 2022-03-22
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0
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38
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June 7, 2026
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Centromeric DEL detected by Manta and visible in coverage, but missing from gnomAD-SV
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2
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81
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June 6, 2026
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Homozygotes enrichment in repeated regions
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0
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46
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May 31, 2026
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Gnomad V4.1.1 Update Missing Constraint Metrics from V4.1.0
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1
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170
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May 28, 2026
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V4.1.1 variant md5sums outdated
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2
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73
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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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65
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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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91
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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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74
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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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46
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May 8, 2026
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BLK duplication variants
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2
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103
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May 4, 2026
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Structural variants
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1
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86
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May 4, 2026
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Skewed sex distribution of SVs in PAR1
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2
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76
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May 4, 2026
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