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X:47308837 G / A


Warning! This variant is only covered in 36138 individuals (adjusted allele number = 72277).
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
rs104894955
Allele Frequency
0.0004842
Filtering AF
0.000671 (European (Non-Finnish))
Allele Count
35 / 72277
UCSC
X-47308837-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.

Population Frequencies
Population Allele Count Allele Number Number of Homozygotes Number of Hemizygotes Allele Frequency
European (Non-Finnish) 35 38498 0 6 0.0009091
East Asian 0 5627 0 0 0
Other 0 526 0 0 0
African 0 7509 0 0 0
Latino 0 7902 0 0 0
South Asian 0 8410 0 0 0
European (Finnish) 0 3805 0 0 0
Total 35 72277 0 6 0.0004842

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.