Interested in working on the development of this resource? Apply here.

10:81697818 A / G


Filter Status
PASS
dbSNP
rs1051246
Allele Frequency
0.1535
Filtering AF
0.2904 (Latino)
Allele Count
18634 / 121392
UCSC
10-81697818-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 3 transcripts in 2 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) 8595 66724 595 0.1288
East Asian 137 8654 2 0.01583
Other 143 908 14 0.1575
African 2483 10406 279 0.2386
Latino 3458 11576 512 0.2987
South Asian 3354 16510 358 0.2031
European (Finnish) 464 6614 18 0.07015
Total 18634 121392 1778 0.1535

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.