Note: This variant is multiallelic! The other alt alleles are:

Warning! This variant is only covered in 443 individuals (adjusted allele number = 886).
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
rs1255251003
Allele Frequency
0.4819
Allele Count
427 / 886
UCSC
17-43066424-CA-C
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
172
Homozygote Number
146
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 0.5053
Yao 0.3667
Dong 0.425
Bouyei 0.3704
Gelao 0.4359
Zhuang 0.4333
Sui 0.3875
Yi 0.4375
Bai 0.5167
Tujia 0.4487
Hui 0.55
Total 0.481941
Population Frequency
Africa/African-American N/A
Ashkenazi Jewish N/A
East Asian N/A
Finnish N/A
Non-Finnish European N/A
OTH N/A
Population Frequency
Africa/African-American N/A
Admixed American/Latino N/A
East Asian N/A
European N/A