rs11145465
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11145465(A;A) |
| Make rs11145465(A;C) |
| Make rs11145465(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 69151677 |
| Gene | TJP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11145465 |
| dbSNP (classic) | rs11145465 |
| ClinGen | rs11145465 |
| ebi | rs11145465 |
| HLI | rs11145465 |
| Exac | rs11145465 |
| Gnomad | rs11145465 |
| Varsome | rs11145465 |
| LitVar | rs11145465 |
| Map | rs11145465 |
| PheGenI | rs11145465 |
| Biobank | rs11145465 |
| 1000 genomes | rs11145465 |
| hgdp | rs11145465 |
| ensembl | rs11145465 |
| geneview | rs11145465 |
| scholar | rs11145465 |
| rs11145465 | |
| pharmgkb | rs11145465 |
| gwascentral | rs11145465 |
| openSNP | rs11145465 |
| 23andMe | rs11145465 |
| SNPshot | rs11145465 |
| SNPdbe | rs11145465 |
| MSV3d | rs11145465 |
| GWAS Ctlg | rs11145465 |
| GMAF | 0.1322 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23396134 |
| Trait | Refractive error |
| Title | Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. |
| Risk Allele | A |
| P-val | 7E-9 |
| Odds Ratio | .12 [0.083-0.165] unit decrease |
