rs112587690
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs112587690(-;-) |
| Make rs112587690(-;GGGCCT) |
| Make rs112587690(GGGCCT;GGGCCT) |
| Reference | GRCh37.p5 37.3/135 |
| Chromosome | 11 |
| Position | 534407 |
| Gene | HRAS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs112587690 |
| dbSNP (classic) | rs112587690 |
| ClinGen | rs112587690 |
| ebi | rs112587690 |
| HLI | rs112587690 |
| Exac | rs112587690 |
| Gnomad | rs112587690 |
| Varsome | rs112587690 |
| LitVar | rs112587690 |
| Map | rs112587690 |
| PheGenI | rs112587690 |
| Biobank | rs112587690 |
| 1000 genomes | rs112587690 |
| hgdp | rs112587690 |
| ensembl | rs112587690 |
| geneview | rs112587690 |
| scholar | rs112587690 |
| rs112587690 | |
| pharmgkb | rs112587690 |
| gwascentral | rs112587690 |
| openSNP | rs112587690 |
| 23andMe | rs112587690 |
| SNPshot | rs112587690 |
| SNPdbe | rs112587690 |
| MSV3d | rs112587690 |
| GWAS Ctlg | rs112587690 |
| Status | Deleted |
| Max Magnitude | 0 |
[PMID 22618666
] Association between HRAS rs12628 and rs112587690 polymorphisms with the risk of melanoma in the North American population
