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ExomesGenomesTotal
Filters No dataPassNot in exomes
Allele Count-6724567245
Allele Number-151216151216
Allele Frequency-0.44470.4447
Grpmax Filtering AF
(95% confidence)
-0.5429
European (non-Finnish)
0.5429
European (non-Finnish)
Number of homozygotes-1613416134

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Genetic Ancestry Group Frequencies

61021038217540.5877
3702867624101300.5476
266951227010.5211
4699081120.5165
145294370.4932
90920962040.4337
62881522212640.4131
139034602830.4017
161147922700.3362
106344131613790.2574
XX345347734683400.4465
XY327117387077940.4428
Total67245151216161340.4447
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: 4.69
    • phyloP: 0.386
    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> 80Age02004006008001.00K1.20K1.40K1.60K1.80K2.00K2.20K2.40K2.60K2.80K3.00KVariant 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 variants6.194e+7

    Value: 6.194e+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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