Warning! This variant is only covered in 474 individuals (adjusted allele number = 948).
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
rs10451271
Allele Frequency
0.05063
Allele Count
48 / 948
UCSC
17-43111154-A-G
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
41
Homozygote Number
0
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 0.0532
Yao 0.1333
Dong 0.075
Bouyei 0.0093
Gelao 0
Zhuang 0.05
Sui 0.075
Yi 0.0125
Bai 0.0167
Tujia 0.0513
Hui 0.1
Total 0.0506329
Population Frequency
Africa/African-American 0.440662
Ashkenazi Jewish 0.4
East Asian 0.0448718
Finnish 0.301843
Non-Finnish European 0.405158
OTH 0.348987
Population Frequency
Africa/African-American 0.4546
Admixed American/Latino 0.3487
East Asian 0.0506
European 0.3628