Variant: 17:43041893 A / T

Warning! This variant is only covered in 461 individuals (adjusted allele number = 922).
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
GRCh38
Filter Status
PASS
dbSNP
rs8071278
Allele Frequency
0.4479
Allele Count
413 / 922
UCSC
17-43041893-A-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
171
Homozygote Number
121
 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
Population Frequency
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Population Frequency
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