Variant: 17:41223094 T / C

Warning! This variant is only covered in 459 individuals (adjusted allele number = 918).
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: rs1799966
Allele Frequency: 0.4248
Allele Count: 390 / 918
UCSC: 17-41223094-T-C
ClinVar: Click to search for variant in Clinvar
Heterozygote Number: 142
Homozygote Number: 124

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: 17:41223094 T / C

Variant: 17:41223094 T / C

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