rs7084402
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7084402(A;A) |
| Make rs7084402(A;G) |
| Make rs7084402(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 58505644 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7084402 |
| dbSNP (classic) | rs7084402 |
| ClinGen | rs7084402 |
| ebi | rs7084402 |
| HLI | rs7084402 |
| Exac | rs7084402 |
| Gnomad | rs7084402 |
| Varsome | rs7084402 |
| LitVar | rs7084402 |
| Map | rs7084402 |
| PheGenI | rs7084402 |
| Biobank | rs7084402 |
| 1000 genomes | rs7084402 |
| hgdp | rs7084402 |
| ensembl | rs7084402 |
| geneview | rs7084402 |
| scholar | rs7084402 |
| rs7084402 | |
| pharmgkb | rs7084402 |
| gwascentral | rs7084402 |
| openSNP | rs7084402 |
| 23andMe | rs7084402 |
| SNPshot | rs7084402 |
| SNPdbe | rs7084402 |
| MSV3d | rs7084402 |
| GWAS Ctlg | rs7084402 |
| GMAF | 0.4959 |
| 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 | 2E-13 |
| Odds Ratio | .11 [0.079-0.137] unit decrease |
[PMID 32816751] Genetic associations of myopia severities and endophenotypes in children.
