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X:153002734 C / T


Warning! This variant is only covered in 28373 individuals (adjusted allele number = 56746).
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
rs373127758
Allele Frequency
3.524e-05
Allele Count
2 / 56746
UCSC
X-153002734-C-T
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.

Annotations

This variant falls on 3 transcripts in 2 genes:

Note: This list may not include additional transcripts in the same gene that the variant does not overlap.
Population Frequencies
Population Allele Count Allele Number Number of Homozygotes Number of Hemizygotes Allele Frequency
European (Non-Finnish) 1 30394 0 0 3.29e-05
East Asian 1 4379 0 0 0.0002284
Other 0 392 0 0 0
African 0 5995 0 0 0
Latino 0 6610 0 0 0
South Asian 0 7071 0 0 0
European (Finnish) 0 1905 0 0 0
Total 2 56746 0 0 3.524e-05

Read Data

This interactive IGV.js visualization shows reads that went into calling this variant.


Note:   Read data is not available for this variant.