Variant: 17:43041893 A / T

Warning! This variant is only covered in 461 individuals (adjusted allele number = 922).
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
GRCh38
Filter Status
PASS
dbSNP
rs8071278
Allele Frequency
0.4479
Allele Count
413 / 922
UCSC
17-43041893-A-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
171
Homozygote Number
121
 Note: These are site-level quality metrics: they may be unpredictable for multi-allelic sites.
Annotations
No annotations were found for this variant.
Population Frequencies
Population Frequency
Miao 0.5106
Yao 0.3333
Dong 0.45
Bouyei 0.4259
Gelao 0.5385
Zhuang 0.4333
Sui 0.325
Yi 0.375
Bai 0.2833
Tujia 0.3974
Hui 0.5375
Total 0.447939
Population Frequency
Africa/African-American 0.823098
Ashkenazi Jewish 0.364529
East Asian 0.369884
Finnish 0.406208
Non-Finnish European 0.342671
OTH 0.455981
Population Frequency
Africa/African-American N/A
Admixed American/Latino N/A
East Asian N/A
European N/A

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