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9:21971182 A / C


Warning! This variant is only covered in 41515 individuals (adjusted allele number = 83030).
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
rs104894099
Allele Frequency
1.204e-05
Filtering AF
0 (None)
Allele Count
1 / 83030
UCSC
9-21971182-A-C
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 45320 0 0
East Asian 0 6020 0 0
Other 0 562 0 0
African 0 5240 0 0
Latino 1 8694 0 0.000115
South Asian 0 13674 0 0
European (Finnish) 0 3520 0 0
Total 1 83030 0 1.204e-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.