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
rs708381
Allele Frequency
0.2897
Allele Count
270 / 932
UCSC
17-43102588-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
136
Homozygote Number
67
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
Miao 0.4043
Yao 0.3
Dong 0.1875
Bouyei 0.1944
Gelao 0.2821
Zhuang 0.35
Sui 0.2875
Yi 0.15
Bai 0.2167
Tujia 0.2949
Hui 0.325
Total 0.2897
Population Frequency
Africa/African-American 0.771452
Ashkenazi Jewish 0.695804
East Asian 0.366452
Finnish 0.578443
Non-Finnish European 0.61845
OTH 0.616604
Population Frequency
Africa/African-American 0.8018
Admixed American/Latino 0.7046
East Asian 0.3462
European 0.5765