Warning! This variant is only covered in 390 individuals (adjusted allele number = 780).
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
rs60755906
Allele Frequency
0.2936
Allele Count
229 / 780
UCSC
17-43060158-G-C
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
75
Homozygote Number
77
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 0.2234
Yao 0.15
Dong 0.2625
Bouyei 0.2407
Gelao 0.2564
Zhuang 0.0667
Sui 0.1375
Yi 0.4875
Bai 0.3167
Tujia 0.1667
Hui 0.3125
Total 0.29359
Population Frequency
Africa/African-American 0.455845
Ashkenazi Jewish 0.37931
East Asian 0.412371
Finnish 0.373272
Non-Finnish European 0.411677
OTH 0.393186
Population Frequency
Africa/African-American 0.4811
Admixed American/Latino 0.3415
East Asian 0.4187
European 0.3449