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22:50965067 T / G


Warning! This variant is only covered in 10041 individuals (adjusted allele number = 20082).
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
rs121913036
Allele Frequency
0.0001494
Filtering AF
4.4e-05 (European (Non-Finnish))
Allele Count
3 / 20082
UCSC
22-50965067-T-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) 2 8022 0 0.0002493
East Asian 0 1072 0 0
Other 0 164 0 0
African 0 1566 0 0
Latino 1 940 0 0.001064
South Asian 0 8126 0 0
European (Finnish) 0 192 0 0
Total 3 20082 0 0.0001494

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.