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9:271626 G / T


Warning! This variant is only covered in 10845 individuals (adjusted allele number = 21690).
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
rs192864327
Allele Frequency
0.0001383
Filtering AF
9.3e-05 (European (Non-Finnish))
Allele Count
3 / 21690
UCSC
9-271626-G-T
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) 3 8776 0 0.0003418
East Asian 0 606 0 0
Other 0 242 0 0
African 0 2138 0 0
Latino 0 400 0 0
South Asian 0 7906 0 0
European (Finnish) 0 1622 0 0
Total 3 21690 0 0.0001383

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.