Variant: 17:43130406 C / T

Warning! This variant is only covered in 451 individuals (adjusted allele number = 902).
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_43130406_C_T
Allele Frequency
0.002217
Allele Count
2 / 902
UCSC
17-43130406-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
2
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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