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

Warning! This variant is only covered in 312 individuals (adjusted allele number = 624).
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
rs1469409175
Allele Frequency
0.1106
Allele Count
69 / 624
UCSC
17-43103112-CT-C
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
64
Homozygote Number
90
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 0.2766
Yao 0.1333
Dong 0.075
Bouyei 0.0926
Gelao 0.2436
Zhuang 0.15
Sui 0.1125
Yi 0.0875
Bai 0.2333
Tujia 0.1282
Hui 0.2125
Total 0.110577
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