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6:29911064 A / G

Warning! This variant is found in phase with 6-29911062-A-G in 1 individuals, altering its functional interpretation
.
Warning! This variant is found in phase with 6-29911063-T-A in 1 individuals, altering its functional interpretation
.
Warning! This variant is found in phase with 6-29911063-T-G in 6706 individuals, altering its functional interpretation
.

Warning! This variant is only covered in 44068 individuals (adjusted allele number = 88136).
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
rs1136695
Allele Frequency
0.5541
Filtering AF
0.7324 (Latino)
Allele Count
48834 / 88136
UCSC
6-29911064-A-G
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) 23429 46078 6985 0.5085
East Asian 4012 6584 1445 0.6094
Other 387 688 119 0.5625
African 4540 7520 1446 0.6037
Latino 6202 8292 2488 0.7479
South Asian 8324 14838 2594 0.561
European (Finnish) 1940 4136 542 0.4691
Total 48834 88136 15619 0.5541

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.