rs2969180
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2969180(A;A) |
| Make rs2969180(A;G) |
| Make rs2969180(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 11504584 |
| Gene | SHISA6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2969180 |
| dbSNP (classic) | rs2969180 |
| ClinGen | rs2969180 |
| ebi | rs2969180 |
| HLI | rs2969180 |
| Exac | rs2969180 |
| Gnomad | rs2969180 |
| Varsome | rs2969180 |
| LitVar | rs2969180 |
| Map | rs2969180 |
| PheGenI | rs2969180 |
| Biobank | rs2969180 |
| 1000 genomes | rs2969180 |
| hgdp | rs2969180 |
| ensembl | rs2969180 |
| geneview | rs2969180 |
| scholar | rs2969180 |
| rs2969180 | |
| pharmgkb | rs2969180 |
| gwascentral | rs2969180 |
| openSNP | rs2969180 |
| 23andMe | rs2969180 |
| SNPshot | rs2969180 |
| SNPdbe | rs2969180 |
| MSV3d | rs2969180 |
| GWAS Ctlg | rs2969180 |
| GMAF | 0.3949 |
| 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 | A |
| P-val | 7E-11 |
| Odds Ratio | .10 [0.072-0.13] unit decrease |
[PMID 24014484
] Education Influences the Association between Genetic Variants and Refractive Error: A Meta-analysis of Five Singapore Studies
[PMID 25628894
] Evaluation of four genetic variants in han chinese subjects with high myopia
