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1:11846252 G / A


Exomes
Genomes
Total
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Allele Count
Allele Number
Allele Frequency
dbSNP
rs4846048
UCSC
1-11846252-G-A
ClinVar
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Note: Plot may include low-quality genotypes that were excluded from allele counts in the table above
Exomes
Genomes

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

This variant falls on 10 transcripts in 2 genes:

Note: This list may not include additional transcripts in the same gene that the variant does not overlap.
Population Frequencies
Population Allele Count Allele Number Number of Homozygotes Allele Frequency
European (Non-Finnish)
Ashkenazi Jewish*
East Asian
Other
African
Latino
South Asian
European (Finnish)
Total
Include:

Read Data

This interactive IGV.js visualization shows reads that went into calling this variant.
Note: These are reassembled reads produced by GATK HaplotypeCaller --bamOutput so they accurately represent what HaplotypeCaller was seeing when it called this variant.





Genomes: