Variant: 17:43087288 G / A

Warning! This variant is only covered in 468 individuals (adjusted allele number = 936).
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
rs544952674
Allele Frequency
0.009615
Allele Count
9 / 936
UCSC
17-43087288-G-A
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
9
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 0.0319
Yao 0.0167
Dong 0
Bouyei 0
Gelao 0
Zhuang 0
Sui 0
Yi 0.0125
Bai 0
Tujia 0.0128
Hui 0
Total 0.00961538
Population Frequency
Africa/African-American N/A
Ashkenazi Jewish N/A
East Asian 0.00833333
Finnish N/A
Non-Finnish European N/A
OTH N/A
Population Frequency
Africa/African-American 0
Admixed American/Latino 0
East Asian 0.0099
European 0

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