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ExomesGenomesTotal
Filters No dataPassNot in exomes
Allele Count-191191
Allele Number-152262152262
Allele Frequency-0.0012540.001254
Grpmax Filtering AF
(95% confidence)
-0.02971
East Asian
0.02971
East Asian
Number of homozygotes-44

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Genetic Ancestry Group Frequencies

175517830.03380
4483200.0008278
91529010.0005886
1211400.0004730
24154000.00004815
0347000.000
01060600.000
029400.000
06802600.000
091200.000
XX907780610.001157
XY1017445630.001357
Total19115226240.001254
Include:

Related Variants

Liftover

The following GRCh37 variant lifts over to this variant:

Variant Effect Predictor

This variant falls on 0 transcripts in 0 genes.

Note The gene symbols shown below are provided by VEP and may differ from the symbol shown on gene pages.

    In Silico Predictors

    • CADD: 1.78
    • phyloP: 0.340
    Note For more detailed and up to date SpliceAI and Pangolin predictions, please visit our SpliceAI Lookup browser

    Genomic Constraint of Surrounding 1kb Region

    This variant does not have non coding constraint data for the surrounding region.

    Age Distribution

    • Exome
    • Genome
    • Variant carriers
    • All individuals
    < 3030-3535-4040-4545-5050-5555-6060-6565-7070-7575-80> 80Age0246810121416182022Variant carriers05001.00K1.50K2.00K2.50K3.00K3.50K4.00KAll individuals

    Genotype Quality Metrics

    • Exome
    • Genome
    • Variant carriers
    • All individuals
    0-510-1520-2530-3540-4550-5560-6570-7580-8590-95> 100Genotype quality020406080100120140160180Variant carriers02.00K4.00K6.00K8.00K10.0K12.0K14.0K16.0K18.0K20.0K22.0K24.0K26.0K28.0K30.0KAll individuals

    Site Quality Metrics

    • Exome
    • Genome
    1e11e1.51e21e2.51e31e3.51e41e4.51e51e5.51e61e6.51e71e7.51e81e8.51e91e9.51e10SiteQuality0200K400K600K800K1.00M1.20M1.40M1.60M1.80M2.00M2.20M2.40M2.60M2.80MGenome variants2.028e+5

    Value: 2.028e+5 (genome samples)

    Site quality approximation for all variants with 0.001 <= AF < 0.002.

    Note: These are site-level quality metrics, they may be unpredictable for multi-allelic sites.

    Read Data


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