Variant: 17:43109057 C / T

Warning! This variant is only covered in 466 individuals (adjusted allele number = 932).
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
rs77323994
Allele Frequency
0.06867
Allele Count
64 / 932
UCSC
17-43109057-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
38
Homozygote Number
13
 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
{{pop.population}} {{pop.af}}
Total {{variant.allele_freq}}
Population Frequency
{{pop.population}} {{pop.af}}
Population Frequency
{{pop.population}} {{pop.af}}

Links

Contact Us

Building No.11, Beishan Industrial Zone,
Yantian District, Shenzhen
Email: GMGD@service.genomics.cn
©2023 BGI - All Rights Reserved ©粤ICP备10059378号-4