Warning! This variant is only covered in 472 individuals (adjusted allele number = 944).
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
rs3024286
Allele Frequency
0.04873
Allele Count
46 / 944
UCSC
17-43040414-G-A
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
36
Homozygote Number
5
Note: These are site-level quality metrics: they may be unpredictable for multi-allelic sites.
Annotations
No annotations were found for this variant.
Population Frequencies
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