rs12229663
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12229663(A;A) |
| Make rs12229663(A;G) |
| Make rs12229663(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 70856216 |
| Gene | PTPRR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12229663 |
| dbSNP (classic) | rs12229663 |
| ClinGen | rs12229663 |
| ebi | rs12229663 |
| HLI | rs12229663 |
| Exac | rs12229663 |
| Gnomad | rs12229663 |
| Varsome | rs12229663 |
| LitVar | rs12229663 |
| Map | rs12229663 |
| PheGenI | rs12229663 |
| Biobank | rs12229663 |
| 1000 genomes | rs12229663 |
| hgdp | rs12229663 |
| ensembl | rs12229663 |
| geneview | rs12229663 |
| scholar | rs12229663 |
| rs12229663 | |
| pharmgkb | rs12229663 |
| gwascentral | rs12229663 |
| openSNP | rs12229663 |
| 23andMe | rs12229663 |
| SNPshot | rs12229663 |
| SNPdbe | rs12229663 |
| MSV3d | rs12229663 |
| GWAS Ctlg | rs12229663 |
| GMAF | 0.2498 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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 | G |
| P-val | 5E-9 |
| Odds Ratio | .10 [0.066-0.132] unit increase |
