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Welcome to gnomAD! :wave:
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0
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736
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June 27, 2023
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About the General category
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0
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190
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June 27, 2023
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File containing binned methylation level of SNVs
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3
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14
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September 6, 2024
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Is joint (combined genome+exome) FAF unreliable if either genome or exome fails filters?
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2
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310
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September 6, 2024
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AB_MEDIAN field in older gnomad releases r2. and 3?
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1
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187
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September 6, 2024
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Rare and common variants numbers
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1
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88
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September 6, 2024
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Number of NFE male individuals in v2.1.1
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4
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191
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September 6, 2024
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Discrepant frequencies flag in VCF files?
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1
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103
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September 5, 2024
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How to contribute with WGS data representing population cohort from Slovakia?
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1
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11
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September 5, 2024
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chrX_mean_dp and chrY_mean_dp
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1
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177
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September 5, 2024
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Haplotype aggregated info
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1
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7
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September 5, 2024
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Difference Between Gene Name and Genomic Position Queries in gnomAD
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0
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6
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September 5, 2024
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Multi-SNV Variant Type
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1
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229
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September 4, 2024
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gnomAD Copy number variants bed files
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3
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29
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September 3, 2024
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V4 vs v4-nonUKB CFTR F508del
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0
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14
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August 30, 2024
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Difference between V2 and V4
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1
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27
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August 27, 2024
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Availability of ExAC WES BAM files
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1
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17
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August 22, 2024
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Query Regarding Overlap Between Exome and Genome Cohorts
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1
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20
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August 22, 2024
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Differences for LC_pLoF flags between v4.1.0 and v2.1.1
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0
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26
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July 30, 2024
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Only need VCFs of healthy individuals
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1
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81
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July 29, 2024
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dbSNP156 vs gnomAD WGS
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0
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19
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July 29, 2024
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Number of expected and observed pLoF variants for CYP8B1 looks unusual
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3
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45
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July 24, 2024
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Number of variants in each vcf file
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2
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69
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July 23, 2024
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V4: Number of missense variants in VCFs doesn't match the stats
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1
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31
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July 23, 2024
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The Genetic Ancestry Group Frequencies table show Amish for v4.1 Exomes
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1
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22
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July 22, 2024
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PhyloP Question- Different on UCSC browser
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1
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73
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July 11, 2024
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GnomAD v3 random forest performance
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0
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56
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July 4, 2024
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Will there be a V4 non-cancer
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2
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75
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July 3, 2024
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List of variants databases
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1
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108
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July 2, 2024
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XX and XY sample numbers for v4 exomes and genomes
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1
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96
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June 28, 2024
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