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11:2167618 A / G


Filter Status
PASS
dbSNP
rs1003484
Allele Frequency
0.6848
Filtering AF
0.8259 (Latino)
Allele Count
81999 / 119736
UCSC
11-2167618-A-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.

Annotations

This variant falls on 8 transcripts in 3 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) 48660 66226 17968 0.7348
East Asian 3869 8446 881 0.4581
Other 618 892 218 0.6928
African 5514 9636 1570 0.5722
Latino 9651 11490 4078 0.8399
South Asian 8701 16464 2353 0.5285
European (Finnish) 4986 6582 1884 0.7575
Total 81999 119736 28952 0.6848

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.