rs79556279
From SNPedia
| (T) allele has increased risk of Behçet's disease |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| (G;T) | 4.11 | increased risk of Behçet's disease |
| (T;T) | 4.11 | increased risk of Behçet's disease |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 6 |
| Position | 31362069 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs79556279 |
| dbSNP (classic) | rs79556279 |
| ClinGen | rs79556279 |
| ebi | rs79556279 |
| HLI | rs79556279 |
| Exac | rs79556279 |
| Gnomad | rs79556279 |
| Varsome | rs79556279 |
| LitVar | rs79556279 |
| Map | rs79556279 |
| PheGenI | rs79556279 |
| Biobank | rs79556279 |
| 1000 genomes | rs79556279 |
| hgdp | rs79556279 |
| ensembl | rs79556279 |
| geneview | rs79556279 |
| scholar | rs79556279 |
| rs79556279 | |
| pharmgkb | rs79556279 |
| gwascentral | rs79556279 |
| openSNP | rs79556279 |
| 23andMe | rs79556279 |
| SNPshot | rs79556279 |
| SNPdbe | rs79556279 |
| MSV3d | rs79556279 |
| GWAS Ctlg | rs79556279 |
| Max Magnitude | 4.11 |
Primary risk for Behçet's disease associated with the minor (T) allele of rs79556279 [PMID 24821759
] [PMID 24876276] [PMID 24286189]
A meta-analysis totaling ~5,000 Behçet's disease (BD) patients from 78 independent studies calculated a pooled odds ratio of 5.78 (CI: 5.0-6.7) for HLA-B51/B5 allele carriers to develop BD compared with noncarriers.[PMID 19790126]
