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19:6713262 G / A


Filter Status
PASS
dbSNP
rs1047286
Allele Frequency
0.1429
Filtering AF
0.1978 (European (Non-Finnish))
Allele Count
17255 / 120776
UCSC
19-6713262-G-A
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 7 transcripts in 1 genes:

missense
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) 13307 66306 1349 0.2007
East Asian 3 8638 0 0.0003473
Other 155 902 19 0.1718
African 349 10304 5 0.03387
Latino 797 11540 30 0.06906
South Asian 1606 16502 90 0.09732
European (Finnish) 1038 6584 79 0.1577
Total 17255 120776 1572 0.1429

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.