Variant: 17:43042192 C / T

Warning! This variant is only covered in 389 individuals (adjusted allele number = 778).
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
rs2981585
Allele Frequency
0.3368
Allele Count
262 / 778
UCSC
17-43042192-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
82
Homozygote Number
90
 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 0.1968
Yao 0.3667
Dong 0.125
Bouyei 0.3519
Gelao 0.2564
Zhuang 0.4
Sui 0.1625
Yi 0.325
Bai 0.2667
Tujia 0.359
Hui 0.35
Total 0.336761
Population Frequency
Africa/African-American 0.878195
Ashkenazi Jewish 0.558621
East Asian 0.523748
Finnish 0.525073
Non-Finnish European 0.558135
OTH 0.571161
Population Frequency
Africa/African-American 0.9289
Admixed American/Latino 0.5014
East Asian 0.4792
European 0.497

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