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9:130565267 A / G


Warning! This variant is only covered in 4086 individuals (adjusted allele number = 8172).
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
PASS
dbSNP
rs10760502
Allele Frequency
0.6782
Filtering AF
0.8421 (East Asian)
Allele Count
5542 / 8172
UCSC
9-130565267-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.

Population Frequencies
Population Allele Count Allele Number Number of Homozygotes Allele Frequency
European (Non-Finnish) 1219 1976 346 0.6169
East Asian 122 124 60 0.9839
Other 72 98 27 0.7347
African 213 256 87 0.832
Latino 64 90 22 0.7111
South Asian 3847 5622 1267 0.6843
European (Finnish) 5 6 2 0.8333
Total 5542 8172 1811 0.6782

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.