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1:201328373 G / A


Warning! This variant is only covered in 46614 individuals (adjusted allele number = 93228).
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
rs121964857
Allele Frequency
0.0004291
Filtering AF
0.000447 (European (Non-Finnish))
Allele Count
40 / 93228
UCSC
1-201328373-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) 33 53974 0 0.0006114
East Asian 0 6754 0 0
Other 1 618 0 0.001618
African 3 8190 0 0.0003663
Latino 2 7520 0 0.000266
South Asian 0 12286 0 0
European (Finnish) 1 3886 0 0.0002573
Total 40 93228 0 0.0004291

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.