rs12205363
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 |
| Make rs12205363(C;C) |
| Make rs12205363(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 129513484 |
| Gene | LAMA2, LOC102723409 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12205363 |
| dbSNP (classic) | rs12205363 |
| ClinGen | rs12205363 |
| ebi | rs12205363 |
| HLI | rs12205363 |
| Exac | rs12205363 |
| Gnomad | rs12205363 |
| Varsome | rs12205363 |
| LitVar | rs12205363 |
| Map | rs12205363 |
| PheGenI | rs12205363 |
| Biobank | rs12205363 |
| 1000 genomes | rs12205363 |
| hgdp | rs12205363 |
| ensembl | rs12205363 |
| geneview | rs12205363 |
| scholar | rs12205363 |
| rs12205363 | |
| pharmgkb | rs12205363 |
| gwascentral | rs12205363 |
| openSNP | rs12205363 |
| 23andMe | rs12205363 |
| SNPshot | rs12205363 |
| SNPdbe | rs12205363 |
| MSV3d | rs12205363 |
| GWAS Ctlg | rs12205363 |
| GMAF | 0.03673 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | C |
| P-val | 2E-12 |
| Odds Ratio | .24 [0.17-0.3] unit increase |
Occurs within the LAMA2 (Laminin alpha-2) gene
