Warning! This variant is only covered in 465 individuals (adjusted allele number = 930).
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
rs12603364
Allele Frequency
0.03118
Allele Count
29 / 930
UCSC
17-43117476-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
25
Homozygote Number
2
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 0.0372
Yao 0
Dong 0.0375
Bouyei 0.0278
Gelao 0.0513
Zhuang 0.0833
Sui 0
Yi 0
Bai 0.0167
Tujia 0.0641
Hui 0.0125
Total 0.0311828
Population Frequency
Africa/African-American 0.0306687
Ashkenazi Jewish 0.163043
East Asian 0.114434
Finnish 0.152941
Non-Finnish European 0.126605
OTH 0.119388
Population Frequency
Africa/African-American 0.0121
Admixed American/Latino 0.111
East Asian 0.1081
European 0.1074