Variant: 17:43057585 C / T

Warning! This variant is only covered in 444 individuals (adjusted allele number = 888).
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
rs11871217
Allele Frequency
0.4043
Allele Count
359 / 888
UCSC
17-43057585-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
123
Homozygote Number
118
 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 0.3564
Yao 0.8
Dong 0.3375
Bouyei 0.4444
Gelao 0.3846
Zhuang 0.3333
Sui 0.3125
Yi 0.2875
Bai 0.4
Tujia 0.2949
Hui 0.3
Total 0.404279
Population Frequency
Africa/African-American 0.244762
Ashkenazi Jewish 0.403448
East Asian 0.454075
Finnish 0.309977
Non-Finnish European 0.329755
OTH 0.322878
Population Frequency
Africa/African-American 0.2451
Admixed American/Latino 0.3746
East Asian 0.4692
European 0.3648

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