Variant: 17:43125629 C / T

Warning! This variant is only covered in 475 individuals (adjusted allele number = 950).
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
rs1411079948
Allele Frequency
0.002105
Allele Count
2 / 950
UCSC
17-43125629-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
{{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