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21:27269932 C / T


Filter Status
PASS
dbSNP
rs63750847
Allele Frequency
0.0004695
Filtering AF
0.0004 (European (Non-Finnish))
Allele Count
57 / 121408
UCSC
21-27269932-C-T
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) 36 66738 0 0.0005394
East Asian 0 8654 0 0
Other 3 908 0 0.003304
African 0 10406 0 0
Latino 0 11578 0 0
South Asian 0 16510 0 0
European (Finnish) 18 6614 0 0.002721
Total 57 121408 0 0.0004695

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.