Variant: 17:43126634 A / G

Warning! This variant is only covered in 471 individuals (adjusted allele number = 942).
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: rs372638484
Allele Frequency: 0.001062
Allele Count: 1 / 942
UCSC: 17-43126634-A-G
ClinVar: Click to search for variant in Clinvar
Heterozygote Number: 1
Homozygote Number: 0

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: 17:43126634 A / G

Variant: 17:43126634 A / G

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