rs9259013
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9259013(A;A) |
| Make rs9259013(A;T) |
| Make rs9259013(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 6 |
| Position | 29874690 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9259013 |
| dbSNP (classic) | rs9259013 |
| ClinGen | rs9259013 |
| ebi | rs9259013 |
| HLI | rs9259013 |
| Exac | rs9259013 |
| Gnomad | rs9259013 |
| Varsome | rs9259013 |
| LitVar | rs9259013 |
| Map | rs9259013 |
| PheGenI | rs9259013 |
| Biobank | rs9259013 |
| 1000 genomes | rs9259013 |
| hgdp | rs9259013 |
| ensembl | rs9259013 |
| geneview | rs9259013 |
| scholar | rs9259013 |
| rs9259013 | |
| pharmgkb | rs9259013 |
| gwascentral | rs9259013 |
| openSNP | rs9259013 |
| 23andMe | rs9259013 |
| SNPshot | rs9259013 |
| SNPdbe | rs9259013 |
| MSV3d | rs9259013 |
| GWAS Ctlg | rs9259013 |
| Merged from | Rs112166594 |
| Max Magnitude | 0 |
Formerly known as rs112166594 and associated with Behçet's disease [PMID 24821759
]
