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10:104934709 T / C


Filter Status
PASS
dbSNP
rs10883841
Allele Frequency
0.1138
Filtering AF
0.1425 (European (Non-Finnish))
Allele Count
13808 / 121330
UCSC
10-104934709-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) 9669 66700 668 0.145
East Asian 1211 8644 100 0.1401
Other 107 908 9 0.1178
African 316 10386 7 0.03043
Latino 818 11570 33 0.0707
South Asian 599 16510 15 0.03628
European (Finnish) 1088 6612 92 0.1645
Total 13808 121330 924 0.1138

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.