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1:156106982 G / A


Warning! This variant is only covered in 35619 individuals (adjusted allele number = 71238).
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
rs201583907
Allele Frequency
0.0001123
Filtering AF
8.5e-05 (European (Non-Finnish))
Allele Count
8 / 71238
UCSC
1-156106982-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) 7 38488 0 0.0001819
East Asian 0 4856 0 0
Other 0 562 0 0
African 1 6832 0 0.0001464
Latino 0 5380 0 0
South Asian 0 12102 0 0
European (Finnish) 0 3018 0 0
Total 8 71238 0 0.0001123

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.