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19:11224181 C / T


Filter Status
PASS
dbSNP
rs1003723
Allele Frequency
0.3858
Filtering AF
0.4403 (European (Non-Finnish))
Allele Count
46433 / 120346
UCSC
19-11224181-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.

Annotations

This variant falls on 10 transcripts in 1 genes:

Note: This list may not include additional transcripts in the same gene that the variant does not overlap.
Population Frequencies
Population Allele Count Allele Number Number of Homozygotes Allele Frequency
European (Non-Finnish) 29370 66064 6511 0.4446
East Asian 1462 8558 114 0.1708
Other 366 902 82 0.4058
African 878 10304 39 0.08521
Latino 4733 11462 1005 0.4129
South Asian 6338 16488 1246 0.3844
European (Finnish) 3286 6568 839 0.5003
Total 46433 120346 9836 0.3858

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.