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22:46615880 T / C

Note: This variant is multiallelic! The other alt alleles are:

Filter Status
PASS
dbSNP
rs1800234
Allele Frequency
0.009613
Filtering AF
0.05274 (Latino)
Allele Count
1163 / 120986
UCSC
22-46615880-T-C
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) 73 66602 0 0.001096
East Asian 361 8618 8 0.04189
Other 10 904 0 0.01106
African 6 10294 0 0.0005829
Latino 649 11522 28 0.05633
South Asian 42 16440 2 0.002555
European (Finnish) 22 6606 1 0.00333
Total 1163 120986 39 0.009613

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.