rs112166594
From SNPedia
| Merged into | rs9259013 |
| Orientation | plus |
| Make rs112166594(A;A) |
| Make rs112166594(A;T) |
| Make rs112166594(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 6 |
| Position | 29874690 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs112166594 |
| dbSNP (classic) | rs112166594 |
| ClinGen | rs112166594 |
| ebi | rs112166594 |
| HLI | rs112166594 |
| Exac | rs112166594 |
| Gnomad | rs112166594 |
| Varsome | rs112166594 |
| LitVar | rs112166594 |
| Map | rs112166594 |
| PheGenI | rs112166594 |
| Biobank | rs112166594 |
| 1000 genomes | rs112166594 |
| hgdp | rs112166594 |
| ensembl | rs112166594 |
| geneview | rs112166594 |
| scholar | rs112166594 |
| rs112166594 | |
| pharmgkb | rs112166594 |
| gwascentral | rs112166594 |
| openSNP | rs112166594 |
| 23andMe | rs112166594 |
| SNPshot | rs112166594 |
| SNPdbe | rs112166594 |
| MSV3d | rs112166594 |
| GWAS Ctlg | rs112166594 |
| Status | Merged into rs9259013 |
| Max Magnitude | 0 |
associated with Behçet's disease [PMID 24821759
]
