Warning! This variant is only covered in 472 individuals (adjusted allele number = 944).
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
rs12450587
Allele Frequency
0.01589
Allele Count
15 / 944
UCSC
17-43108899-G-C
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
11
Homozygote Number
2
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 0.0053
Yao 0.0667
Dong 0.0375
Bouyei 0
Gelao 0
Zhuang 0.0333
Sui 0.0125
Yi 0
Bai 0
Tujia 0
Hui 0.05
Total 0.0158898
Population Frequency
Africa/African-American 0.0833142
Ashkenazi Jewish 0.224138
East Asian 0.0134961
Finnish 0.146805
Non-Finnish European 0.199039
OTH 0.169118
Population Frequency
Africa/African-American 0.0628
Admixed American/Latino 0.2075
East Asian 0.0159
European 0.1928