Variant: 17:43126431 C / G

Warning! This variant is only covered in 470 individuals (adjusted allele number = 940).
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
chr17_43126431_C_G
Allele Frequency
0.001064
Allele Count
1 / 940
UCSC
17-43126431-C-G
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
1
Homozygote Number
0
 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
Population Frequency
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Population Frequency
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Population Frequency
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