Interested in working on the development of this resource? Apply here.

2:167163041 G / A

Warning! This variant is only covered in 17291 individuals (adjusted allele number = 34582).
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
Allele Frequency
Filtering AF
0 (None)
Allele Count
1 / 34582
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 16612 0 6.02e-05
East Asian 0 2182 0 0
Other 0 344 0 0
African 0 3596 0 0
Latino 0 1246 0 0
South Asian 0 8496 0 0
European (Finnish) 0 2106 0 0
Total 1 34582 0 2.892e-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.