Variant: 17:43072190 C / 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
rs733511
Allele Frequency
0.1165
Allele Count
109 / 936
UCSC
17-43072190-C-A
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
87
Homozygote Number
11
 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 0.1277
Yao 0.0167
Dong 0.05
Bouyei 0.1204
Gelao 0.0897
Zhuang 0.15
Sui 0.2
Yi 0.0875
Bai 0.1833
Tujia 0.0897
Hui 0.125
Total 0.116453
Population Frequency
Africa/African-American 0.00172216
Ashkenazi Jewish 0.00689655
East Asian 0.133504
Finnish 0.0129459
Non-Finnish European 0.00181418
OTH 0.0137868
Population Frequency
Africa/African-American 0.0008
Admixed American/Latino 0.1153
East Asian 0.1319
European 0.003

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