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

Warning! This variant is only covered in 227 individuals (adjusted allele number = 454).
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
rs1413268051
Allele Frequency
0.02863
Allele Count
13 / 454
UCSC
17-43100971-T-TAAA
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
14
Homozygote Number
21
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 0.016
Yao 0.0833
Dong 0.025
Bouyei 0
Gelao 0
Zhuang 0
Sui 0
Yi 0.025
Bai 0
Tujia 0.0128
Hui 0
Total 0.0286344
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