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

Warning! This variant is only covered in 464 individuals (adjusted allele number = 928).
This means that the site is covered in fewer than 80% of the individuals in GMGD, which may indicate a low-quality site.


Genome build
GRCh37
Filter Status
PASS
dbSNP
rs11290490
Allele Frequency
0.2252
Allele Count
209 / 928
UCSC
17-43124499-GA-G
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
109
Homozygote Number
52
Note: These are site-level quality metrics: they may be unpredictable for multi-allelic sites.
Annotations

This variant falls on 1 transcripts in 1 genes:

Note: This list may not include additional transcripts in the same gene that the variant does not overlap.
Population Frequencies
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