Variant: 17:43041954 C / T

Warning! This variant is only covered in 455 individuals (adjusted allele number = 910).
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
rs2981586
Allele Frequency
0.3681
Allele Count
335 / 910
UCSC
17-43041954-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
141
Homozygote Number
97
 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 0.2394
Yao 0.3
Dong 0.3
Bouyei 0.4352
Gelao 0.2821
Zhuang 0.4167
Sui 0.325
Yi 0.4875
Bai 0.3333
Tujia 0.4103
Hui 0.4625
Total 0.368132
Population Frequency
Africa/African-American 0.879334
Ashkenazi Jewish 0.558621
East Asian 0.521935
Finnish 0.523933
Non-Finnish European 0.558245
OTH 0.56814
Population Frequency
Africa/African-American 0.9304
Admixed American/Latino 0.5014
East Asian 0.4821
European 0.497

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