rs4778879
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4778879(A;A) |
| Make rs4778879(A;G) |
| Make rs4778879(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 79080533 |
| Gene | RASGRF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4778879 |
| dbSNP (classic) | rs4778879 |
| ClinGen | rs4778879 |
| ebi | rs4778879 |
| HLI | rs4778879 |
| Exac | rs4778879 |
| Gnomad | rs4778879 |
| Varsome | rs4778879 |
| LitVar | rs4778879 |
| Map | rs4778879 |
| PheGenI | rs4778879 |
| Biobank | rs4778879 |
| 1000 genomes | rs4778879 |
| hgdp | rs4778879 |
| ensembl | rs4778879 |
| geneview | rs4778879 |
| scholar | rs4778879 |
| rs4778879 | |
| pharmgkb | rs4778879 |
| gwascentral | rs4778879 |
| openSNP | rs4778879 |
| 23andMe | rs4778879 |
| SNPshot | rs4778879 |
| SNPdbe | rs4778879 |
| MSV3d | rs4778879 |
| GWAS Ctlg | rs4778879 |
| GMAF | 0.4513 |
| 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 | 4E-11 |
| Odds Ratio | .10 [0.073-0.131] unit decrease |
