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22:51065766 G / A


Warning! This variant is only covered in 26720 individuals (adjusted allele number = 53440).
This means that the site is covered in fewer than 80% of the individuals in ExAC, which may indicate a low-quality site.


Filter Status
PASS
dbSNP
rs74315456
Allele Frequency
1.871e-05
Filtering AF
0 (None)
Allele Count
1 / 53440
UCSC
22-51065766-G-A
ClinVar
Click to search for variant in Clinvar
Note: Plot may include low-quality genotypes that were excluded from allele counts in the table above

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

Population Frequencies
Population Allele Count Allele Number Number of Homozygotes Allele Frequency
European (Non-Finnish) 1 28890 0 3.461e-05
East Asian 0 3738 0 0
Other 0 368 0 0
African 0 3896 0 0
Latino 0 3662 0 0
South Asian 0 11308 0 0
European (Finnish) 0 1578 0 0
Total 1 53440 0 1.871e-05

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.