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

Warning! This variant is only covered in 212 individuals (adjusted allele number = 424).
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
rs1290322347
Allele Frequency
0.1604
Allele Count
68 / 424
UCSC
17-43063653-GTT-G
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
23
Homozygote Number
40
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 0.0266
Yao 0.0333
Dong 0.025
Bouyei 0.0278
Gelao 0.0256
Zhuang 0
Sui 0
Yi 0
Bai 0
Tujia 0
Hui 0.05
Total 0.160377
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