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2:26683072 G / A


Warning! This variant is only covered in 30527 individuals (adjusted allele number = 61054).
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
rs368790049
Allele Frequency
3.276e-05
Filtering AF
0 (None)
Allele Count
2 / 61054
UCSC
2-26683072-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 33756 0 2.962e-05
East Asian 0 4546 0 0
Other 0 456 0 0
African 1 5778 0 0.0001731
Latino 0 4206 0 0
South Asian 0 10422 0 0
European (Finnish) 0 1890 0 0
Total 2 61054 0 3.276e-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.