rs17648524
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17648524(C;C) |
| Make rs17648524(C;G) |
| Make rs17648524(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 7409682 |
| Gene | RBFOX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17648524 |
| dbSNP (classic) | rs17648524 |
| ClinGen | rs17648524 |
| ebi | rs17648524 |
| HLI | rs17648524 |
| Exac | rs17648524 |
| Gnomad | rs17648524 |
| Varsome | rs17648524 |
| LitVar | rs17648524 |
| Map | rs17648524 |
| PheGenI | rs17648524 |
| Biobank | rs17648524 |
| 1000 genomes | rs17648524 |
| hgdp | rs17648524 |
| ensembl | rs17648524 |
| geneview | rs17648524 |
| scholar | rs17648524 |
| rs17648524 | |
| pharmgkb | rs17648524 |
| gwascentral | rs17648524 |
| openSNP | rs17648524 |
| 23andMe | rs17648524 |
| SNPshot | rs17648524 |
| SNPdbe | rs17648524 |
| MSV3d | rs17648524 |
| GWAS Ctlg | rs17648524 |
| GMAF | 0.2268 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 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 | C |
| P-val | 6E-10 |
| Odds Ratio | .12 [0.081-0.155] unit decrease |
