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Welcome to gnomAD! :wave:
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0
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1036
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June 27, 2023
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PRKCE variant 2-46001442 - G-A (GRCh38)
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2
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35
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November 18, 2025
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Urgent query-Genotype Quality for SVs in gnomAD v4.1.0
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0
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12
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November 12, 2025
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LD in release v5
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1
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26
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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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17
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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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25
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October 27, 2025
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Genotype quality for SV call in v4
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0
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19
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October 10, 2025
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Grpmax Filtering AF field in v2 vcf files
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1
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23
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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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87
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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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27
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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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284
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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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25
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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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41
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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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24
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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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48
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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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60
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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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310
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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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56
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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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57
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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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41
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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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56
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August 19, 2025
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Best Practice for Reporting Population Allele Frequencies When Both UK Biobank and Non-UK Biobank Data Are Available in gnomAD v4
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3
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90
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August 19, 2025
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How to calculate hemizygous counts
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2
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66
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August 19, 2025
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Reference bias in variant calling?
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1
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41
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August 18, 2025
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Tandem Repeat: PRE-MIR7-2
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1
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17
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August 18, 2025
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Gnomad STR dataset genomic coordinates
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1
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27
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August 18, 2025
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VEP annotation for joint VCFs?
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1
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24
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August 18, 2025
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gnomAD v4 rare exome cnv interval list
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1
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33
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August 18, 2025
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Regional Missense Constraint
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1
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41
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August 5, 2025
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Annotating data with the gnomAD variant ID
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3
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472
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July 30, 2025
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