Variant: 17:43087183 G / A

Warning! This variant is only covered in 471 individuals (adjusted allele number = 942).
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
rs35103016
Allele Frequency
0.01274
Allele Count
12 / 942
UCSC
17-43087183-G-A
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
12
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 0.0106
Yao 0.05
Dong 0
Bouyei 0
Gelao 0
Zhuang 0.0333
Sui 0
Yi 0
Bai 0
Tujia 0.0128
Hui 0.05
Total 0.0127389
Population Frequency
Africa/African-American 0.0562069
Ashkenazi Jewish 0.334483
East Asian 0.0160668
Finnish 0.264977
Non-Finnish European 0.293972
OTH 0.264273
Population Frequency
Africa/African-American 0.0166
Admixed American/Latino 0.2536
East Asian 0.0159
European 0.3131

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