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22:30070871 G / A


Warning! This variant is only covered in 11928 individuals (adjusted allele number = 23856).
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
rs74315503
Allele Frequency
0.0003773
Filtering AF
0.001586 (African)
Allele Count
9 / 23856
UCSC
22-30070871-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) 0 10544 0 0
East Asian 0 1214 0 0
Other 0 214 0 0
African 9 2960 0 0.003041
Latino 0 730 0 0
South Asian 0 8024 0 0
European (Finnish) 0 170 0 0
Total 9 23856 0 0.0003773

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.