Variant: 17:43041806 T / C

Warning! This variant is only covered in 464 individuals (adjusted allele number = 928).
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: rs2920452
Allele Frequency: 0.3869
Allele Count: 359 / 928
UCSC: 17-43041806-T-C
ClinVar: Click to search for variant in Clinvar
Heterozygote Number: 173
Homozygote Number: 93

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: 17:43041806 T / C

Variant: 17:43041806 T / C

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