Variant: 17:43127395 A / G

Warning! This variant is only covered in 458 individuals (adjusted allele number = 916).
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: rs28497626
Allele Frequency: 0.1124
Allele Count: 103 / 916
UCSC: 17-43127395-A-G
ClinVar: Click to search for variant in Clinvar
Heterozygote Number: 81
Homozygote Number: 11

Site Quality Metrics

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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Variant: 17:43127395 A / G

Variant: 17:43127395 A / G

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