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17:61574338 C / T


Warning! This variant is only covered in 48094 individuals (adjusted allele number = 96188).
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
rs121912703
Allele Frequency
2.079e-05
Filtering AF
0 (None)
Allele Count
2 / 96188
UCSC
17-61574338-C-T
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) 1 52796 0 1.894e-05
East Asian 0 7016 0 0
Other 0 660 0 0
African 0 8162 0 0
Latino 0 9168 0 0
South Asian 1 14344 0 6.972e-05
European (Finnish) 0 4042 0 0
Total 2 96188 0 2.079e-05

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.