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6:31783755 T / C

Warning! This variant is only covered in 8481 individuals (adjusted allele number = 16962).
This means that the site is covered in fewer than 80% of the individuals in ExAC, which may indicate a low-quality site.

Filter Status
Allele Frequency
Filtering AF
0.9547 (South Asian)
Allele Count
15855 / 16962
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.


This variant falls on 5 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) 7036 7884 3122 0.8924
East Asian 658 668 324 0.985
Other 146 154 70 0.9481
African 1094 1116 536 0.9803
Latino 601 624 289 0.9631
South Asian 5969 6120 2910 0.9753
European (Finnish) 351 396 153 0.8864
Total 15855 16962 7404 0.9347

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.