Variant: 17:43127708 G / A

Warning! This variant is only covered in 468 individuals (adjusted allele number = 936).
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: rs12950988
Allele Frequency: 0.2735
Allele Count: 256 / 936
UCSC: 17-43127708-G-A
ClinVar: Click to search for variant in Clinvar
Heterozygote Number: 137
Homozygote Number: 59

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: 17:43127708 G / A

Variant: 17:43127708 G / A

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