Warning! This variant is only covered in 451 individuals (adjusted allele number = 902).
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
rs4793180
Allele Frequency
0.1608
Allele Count
145 / 902
UCSC
17-43121308-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
85
Homozygote Number
30
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 0.1702
Yao 0.05
Dong 0.025
Bouyei 0.1481
Gelao 0.1923
Zhuang 0.2333
Sui 0.175
Yi 0.1125
Bai 0.2
Tujia 0.1923
Hui 0.1625
Total 0.160754
Population Frequency
Africa/African-American 0.0987824
Ashkenazi Jewish 0.274306
East Asian 0.280284
Finnish 0.242345
Non-Finnish European 0.203367
OTH 0.226937
Population Frequency
Africa/African-American 0.087
Admixed American/Latino 0.2853
East Asian 0.2659
European 0.1978