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16:3304567 C / G


Warning! This variant is only covered in 14587 individuals (adjusted allele number = 29174).
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
rs104895079
Allele Frequency
3.428e-05
Filtering AF
0 (None)
Allele Count
1 / 29174
UCSC
16-3304567-C-G
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 13236 0 7.555e-05
East Asian 0 1704 0 0
Other 0 246 0 0
African 0 1896 0 0
Latino 0 1378 0 0
South Asian 0 9872 0 0
European (Finnish) 0 842 0 0
Total 1 29174 0 3.428e-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.