rs12960119
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12960119(A;A) |
| Make rs12960119(A;G) |
| Make rs12960119(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 26034739 |
| Gene | SS18 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12960119 |
| dbSNP (classic) | rs12960119 |
| ClinGen | rs12960119 |
| ebi | rs12960119 |
| HLI | rs12960119 |
| Exac | rs12960119 |
| Gnomad | rs12960119 |
| Varsome | rs12960119 |
| LitVar | rs12960119 |
| Map | rs12960119 |
| PheGenI | rs12960119 |
| Biobank | rs12960119 |
| 1000 genomes | rs12960119 |
| hgdp | rs12960119 |
| ensembl | rs12960119 |
| geneview | rs12960119 |
| scholar | rs12960119 |
| rs12960119 | |
| pharmgkb | rs12960119 |
| gwascentral | rs12960119 |
| openSNP | rs12960119 |
| 23andMe | rs12960119 |
| SNPshot | rs12960119 |
| SNPdbe | rs12960119 |
| MSV3d | rs12960119 |
| GWAS Ctlg | rs12960119 |
| GMAF | 0.2938 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23585552] Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment
