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1:156107470 G / A


Warning! This variant is only covered in 10787 individuals (adjusted allele number = 21574).
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
rs142191737
Allele Frequency
0.0001854
Filtering AF
8.8e-05 (European (Non-Finnish))
Allele Count
4 / 21574
UCSC
1-156107470-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 Allele Frequency
European (Non-Finnish) 3 9262 0 0.0003239
East Asian 0 870 0 0
Other 0 196 0 0
African 0 2864 0 0
Latino 0 404 0 0
South Asian 1 7920 0 0.0001263
European (Finnish) 0 58 0 0
Total 4 21574 0 0.0001854

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.