rs7837791
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7837791(G;G) |
| Make rs7837791(G;T) |
| Make rs7837791(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 59266527 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7837791 |
| dbSNP (classic) | rs7837791 |
| ClinGen | rs7837791 |
| ebi | rs7837791 |
| HLI | rs7837791 |
| Exac | rs7837791 |
| Gnomad | rs7837791 |
| Varsome | rs7837791 |
| LitVar | rs7837791 |
| Map | rs7837791 |
| PheGenI | rs7837791 |
| Biobank | rs7837791 |
| 1000 genomes | rs7837791 |
| hgdp | rs7837791 |
| ensembl | rs7837791 |
| geneview | rs7837791 |
| scholar | rs7837791 |
| rs7837791 | |
| pharmgkb | rs7837791 |
| gwascentral | rs7837791 |
| openSNP | rs7837791 |
| 23andMe | rs7837791 |
| SNPshot | rs7837791 |
| SNPdbe | rs7837791 |
| MSV3d | rs7837791 |
| GWAS Ctlg | rs7837791 |
| GMAF | 0.4568 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 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 | T |
| P-val | 4E-12 |
| Odds Ratio | .11 [0.077-0.135] unit increase |
[PMID 25628894] Evaluation of four genetic variants in han chinese subjects with high myopia
