PhyloP indel scores
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1
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68
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February 13, 2025
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XX and XY sample numbers for v4 exomes and genomes
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1
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111
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June 28, 2024
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pLoF Metrics by Gene TSV columns
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3
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54
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December 11, 2024
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V4.1 Structural Variants BED files
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1
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64
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July 29, 2024
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Rounding the frequencies in the browser
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3
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53
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September 10, 2024
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What is the estimated relative distribution of gnomAD ancestry groups in the global population?
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1
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84
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June 27, 2024
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gnomAD v.4.1 API?
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1
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58
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January 24, 2025
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File containing binned methylation level of SNVs
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3
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50
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September 6, 2024
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Congenital Heart Defects - Screened out?
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1
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70
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June 27, 2024
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Ancestry RF classifer code and scripts
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5
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38
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March 18, 2025
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Assistance with Querying Non-Synonymous Variants for Specific Transcript ID
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2
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44
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August 9, 2024
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Short range haplotype frequencies
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0
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91
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June 21, 2024
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Access to Download
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1
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49
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October 16, 2024
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RTEL1 Intron 15 - Complex Region
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0
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149
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May 1, 2024
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Geographical place of origin of samples
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1
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47
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September 11, 2024
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GnomAD SVs v4, X-chromosome: homozygous males
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1
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63
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November 5, 2024
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GnomAD v3 random forest performance
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0
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85
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July 4, 2024
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Insertion and Deletion at the same position with flipped alleles
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1
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48
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October 28, 2024
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All-sites allele numbers by ancestry group?
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1
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42
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October 10, 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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50
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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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41
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July 22, 2024
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How to contribute with WGS data representing population cohort from Slovakia?
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2
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33
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September 9, 2024
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Genome build used for gnomad v4.1
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1
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42
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April 8, 2025
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C4B variant, please help!
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1
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43
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February 20, 2025
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How to find germine mutations associated with cancer v 3.1.2
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1
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33
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January 8, 2025
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GnomAD EXOME FILTERED PPM1D Variant
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1
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37
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November 12, 2024
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Haplotype aggregated info
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1
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35
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September 5, 2024
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Availability of ExAC WES BAM files
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1
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39
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August 22, 2024
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How to extract and analyze variant sequences from gnomAD v4 exome VCF
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0
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48
|
January 12, 2025
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Difference Between Gene Name and Genomic Position Queries in gnomAD
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1
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37
|
September 17, 2024
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Feature Suggestion: Proposal to Integrate GeneBe ACMG Criteria in gnomAD
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0
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47
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July 17, 2024
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Co-located variants
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1
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31
|
December 3, 2024
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Query Regarding Overlap Between Exome and Genome Cohorts
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1
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37
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August 22, 2024
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Quality score in gnomAD SVs v4.1.0
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1
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30
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December 18, 2024
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Phased info for STR?
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0
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40
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July 15, 2024
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Mutation rate table
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0
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41
|
July 25, 2024
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Liftover API from grch37 to grch38
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1
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27
|
February 4, 2025
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GnomAD v2.1.1 Regional missense constraint file is incomplete
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1
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37
|
December 3, 2024
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LOEUF score for a particular exon
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1
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30
|
January 31, 2025
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Same indel called as different SNVs
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1
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29
|
December 30, 2024
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How to merge multiple variants into the same CNV?
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0
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40
|
November 13, 2024
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Figure broken in SV gnomAD 4 post
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1
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26
|
January 31, 2025
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Discordant variant observations between v2.1.1 and v4.1
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2
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24
|
April 7, 2025
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Separating healthy populations from those with disease
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0
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36
|
December 3, 2024
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Incompatible gnomAD v4.1.0 vcf for Mutect2
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1
|
25
|
February 28, 2025
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Differences in reference allele counts?
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0
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34
|
October 8, 2024
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Comparing constraint between different population sizes
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0
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30
|
October 1, 2024
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How to calculate MAPS score for gnomAD v4/v4.1?
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0
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40
|
September 19, 2024
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Gene Symbols Starting with 'CA'
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1
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23
|
September 4, 2024
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How can I tell if two variants occur within an individual?
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0
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33
|
February 20, 2025
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