rs955943
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs955943(A;A) |
| Make rs955943(A;G) |
| Make rs955943(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 16512785 |
| Gene | LDB2, LOC105374505 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs955943 |
| dbSNP (classic) | rs955943 |
| ClinGen | rs955943 |
| ebi | rs955943 |
| HLI | rs955943 |
| Exac | rs955943 |
| Gnomad | rs955943 |
| Varsome | rs955943 |
| LitVar | rs955943 |
| Map | rs955943 |
| PheGenI | rs955943 |
| Biobank | rs955943 |
| 1000 genomes | rs955943 |
| hgdp | rs955943 |
| ensembl | rs955943 |
| geneview | rs955943 |
| scholar | rs955943 |
| rs955943 | |
| pharmgkb | rs955943 |
| gwascentral | rs955943 |
| openSNP | rs955943 |
| 23andMe | rs955943 |
| SNPshot | rs955943 |
| SNPdbe | rs955943 |
| MSV3d | rs955943 |
| GWAS Ctlg | rs955943 |
| GMAF | 0.0932 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23585552] |
| Trait | Rhegmatogenous retinal detachment |
| Title | Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment. |
| Risk Allele | A |
| P-val | 5E-6 |
| Odds Ratio | 1.41 [1.21-1.64] |
