rs18030962
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs18030962(G;G) |
| Make rs18030962(G;T) |
| Make rs18030962(T;T) |
| Reference | Build_4.0 5.1/138 |
| Chromosome | 2 |
| Position | 11414344 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs18030962 |
| dbSNP (classic) | rs18030962 |
| ClinGen | rs18030962 |
| ebi | rs18030962 |
| HLI | rs18030962 |
| Exac | rs18030962 |
| Gnomad | rs18030962 |
| Varsome | rs18030962 |
| LitVar | rs18030962 |
| Map | rs18030962 |
| PheGenI | rs18030962 |
| Biobank | rs18030962 |
| 1000 genomes | rs18030962 |
| hgdp | rs18030962 |
| ensembl | rs18030962 |
| geneview | rs18030962 |
| scholar | rs18030962 |
| rs18030962 | |
| pharmgkb | rs18030962 |
| gwascentral | rs18030962 |
| openSNP | rs18030962 |
| 23andMe | rs18030962 |
| SNPshot | rs18030962 |
| SNPdbe | rs18030962 |
| MSV3d | rs18030962 |
| GWAS Ctlg | rs18030962 |
| Max Magnitude | 0 |
[PMID 22759724] Polymorphisms in the melatonin receptor 1B gene and the risk of delirium
