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8:37823798 A / G


Filter Status
PASS
dbSNP
rs4994
Allele Frequency
0.1057
Filtering AF
0.2128 (Latino)
Allele Count
12257 / 115984
UCSC
8-37823798-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 2 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) 4780 63850 197 0.07486
East Asian 1214 8408 87 0.1444
Other 90 824 9 0.1092
African 1071 9512 61 0.1126
Latino 2469 11220 278 0.2201
South Asian 2112 16304 144 0.1295
European (Finnish) 521 5866 21 0.08882
Total 12257 115984 797 0.1057

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.