rs1585471
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1585471(A;A) |
| Make rs1585471(A;G) |
| Make rs1585471(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 111781479 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1585471 |
| dbSNP (classic) | rs1585471 |
| ClinGen | rs1585471 |
| ebi | rs1585471 |
| HLI | rs1585471 |
| Exac | rs1585471 |
| Gnomad | rs1585471 |
| Varsome | rs1585471 |
| LitVar | rs1585471 |
| Map | rs1585471 |
| PheGenI | rs1585471 |
| Biobank | rs1585471 |
| 1000 genomes | rs1585471 |
| hgdp | rs1585471 |
| ensembl | rs1585471 |
| geneview | rs1585471 |
| scholar | rs1585471 |
| rs1585471 | |
| pharmgkb | rs1585471 |
| gwascentral | rs1585471 |
| openSNP | rs1585471 |
| 23andMe | rs1585471 |
| SNPshot | rs1585471 |
| SNPdbe | rs1585471 |
| MSV3d | rs1585471 |
| GWAS Ctlg | rs1585471 |
| GMAF | 0.3503 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21505071] |
| Trait | |
| Title | A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population. |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | 1.1500 [1.09-1.22] |
[PMID 22150588] Common variants in chromosome 4q25 are associated with myopia in Chinese adults.
