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ExomesGenomesTotal
Filters No dataPassNot in exomes
Allele Count-5759257592
Allele Number-151976151976
Allele Frequency-0.37900.3790
Grpmax Filtering AF
(95% confidence)
-0.5644
East Asian
0.5644
East Asian
Number of homozygotes-1222212222

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Genetic Ancestry Group Frequencies

299651508740.5817
52721054013080.5002
426910960.4681
309316793669630.4553
66541528814890.4352
203948184400.4232
83921061700.3984
133634662530.3855
94294160.3197
7005414686130.1689
XX290957770260860.3744
XY284977427461360.3837
Total57592151976122220.3790
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: 0.131
    • phyloP: -2.93
    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> 80Age02004006008001.00K1.20K1.40K1.60K1.80K2.00K2.20K2.40K2.60KVariant 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 quality05.00K10.0K15.0K20.0K25.0K30.0K35.0KVariant carriers05.00K10.0K15.0K20.0K25.0K30.0K35.0KAll individuals

    Site Quality Metrics

    • Exome
    • Genome
    1e11e1.51e21e2.51e31e3.51e41e4.51e51e5.51e61e6.51e71e7.51e81e8.51e91e9.51e10SiteQuality0200K400K600K800K1.00M1.20M1.40MGenome variants5.869e+7

    Value: 5.869e+7 (genome samples)

    Site quality approximation for all variants with 0.2 <= AF < 0.5.

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

    Read Data


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