Variant: 17:43042192 C / T

Warning! This variant is only covered in 389 individuals (adjusted allele number = 778).
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
rs2981585
Allele Frequency
0.3368
Allele Count
262 / 778
UCSC
17-43042192-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
82
Homozygote Number
90
 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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