Warning! This variant is only covered in 458 individuals (adjusted allele number = 916).
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
rs5820564
Allele Frequency
0.3854
Allele Count
353 / 916
UCSC
17-43090043-G-GC
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
143
Homozygote Number
104
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 0.3191
Yao 0.25
Dong 0.3375
Bouyei 0.4907
Gelao 0.2949
Zhuang 0.45
Sui 0.275
Yi 0.325
Bai 0.3333
Tujia 0.4359
Hui 0.575
Total 0.385371
Population Frequency
Africa/African-American 0.449411
Ashkenazi Jewish 0.537931
East Asian 0.513548
Finnish 0.463124
Non-Finnish European 0.492003
OTH 0.478664
Population Frequency
Africa/African-American 0.4236
Admixed American/Latino 0.5663
East Asian 0.505
European 0.496