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19:40903673 G / T


Warning! This variant is only covered in 9989 individuals (adjusted allele number = 19978).
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
AC_Adj0_Filter
dbSNP
rs104894706
Allele Frequency
NA (Allele Number = 0)
Filtering AF
0 (None)
Allele Count
0 / 19978
UCSC
19-40903673-G-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 2 transcripts in 1 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 Allele Frequency
European (Non-Finnish) 0 7886 0 0
East Asian 0 1678 0 0
Other 0 174 0 0
African 0 1520 0 0
Latino 0 404 0 0
South Asian 0 8134 0 0
European (Finnish) 0 182 0 0
Total 0 19978 0 0