Variant: 17:43072663 C / T

Warning! This variant is only covered in 399 individuals (adjusted allele number = 798).
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
rs9900708
Allele Frequency
0.287
Allele Count
229 / 798
UCSC
17-43072663-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
79
Homozygote Number
75
 Note: These are site-level quality metrics: they may be unpredictable for multi-allelic sites.
Annotations

This variant falls on 1 transcripts in 1 genes:

Note: This list may not include additional transcripts in the same gene that the variant does not overlap.
Population Frequencies
Population Frequency
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Population Frequency
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Population Frequency
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Links

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