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
