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9:21971152 T / C


Warning! This variant is only covered in 40813 individuals (adjusted allele number = 81626).
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
rs372670098
Allele Frequency
1.225e-05
Filtering AF
0 (None)
Allele Count
1 / 81626
UCSC
9-21971152-T-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) 1 44184 0 2.263e-05
East Asian 0 6012 0 0
Other 0 562 0 0
African 0 5196 0 0
Latino 0 8460 0 0
South Asian 0 13704 0 0
European (Finnish) 0 3508 0 0
Total 1 81626 0 1.225e-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.