Variant: 17:43102286 A / C

Warning! This variant is only covered in 440 individuals (adjusted allele number = 880).
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
rs730953
Allele Frequency
0.2682
Allele Count
236 / 880
UCSC
17-43102286-A-C
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
105
Homozygote Number
65
 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 0.3298
Yao 0.2667
Dong 0.1625
Bouyei 0.1852
Gelao 0.2692
Zhuang 0.25
Sui 0.2375
Yi 0.175
Bai 0.1833
Tujia 0.2308
Hui 0.3375
Total 0.268182
Population Frequency
Africa/African-American 0.611882
Ashkenazi Jewish 0.693103
East Asian 0.366883
Finnish 0.578216
Non-Finnish European 0.619119
OTH 0.608534
Population Frequency
Africa/African-American 0.618
Admixed American/Latino 0.6945
East Asian 0.3462
European 0.5746

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