rs13382811
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13382811(C;C) |
Make rs13382811(C;T) |
Make rs13382811(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 144466053 |
Gene | ZEB2 |
is a | snp |
is | mentioned by |
dbSNP | rs13382811 |
dbSNP (classic) | rs13382811 |
ClinGen | rs13382811 |
ebi | rs13382811 |
HLI | rs13382811 |
Exac | rs13382811 |
Gnomad | rs13382811 |
Varsome | rs13382811 |
LitVar | rs13382811 |
Map | rs13382811 |
PheGenI | rs13382811 |
Biobank | rs13382811 |
1000 genomes | rs13382811 |
hgdp | rs13382811 |
ensembl | rs13382811 |
geneview | rs13382811 |
scholar | rs13382811 |
rs13382811 | |
pharmgkb | rs13382811 |
gwascentral | rs13382811 |
openSNP | rs13382811 |
23andMe | rs13382811 |
SNPshot | rs13382811 |
SNPdbe | rs13382811 |
MSV3d | rs13382811 |
GWAS Ctlg | rs13382811 |
GMAF | 0.2098 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23933737] |
Trait | Myopia (severe) |
Title | Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia. |
Risk Allele | T |
P-val | 6E-10 |
Odds Ratio | 1.26 [NR] |
[PMID 28848321] Association and interaction of myopia with SNP markers rs13382811 and rs6469937 at ZFHX1B and SNTB1 in Han Chinese and European populations.
[PMID 31300455] Association of the ZC3H11B, ZFHX1B and SNTB1 genes with myopia of different severities.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2c
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip Ancestry v2d