rs79556279(T;T)
From SNPedia
| increased risk of Behçet's disease |
| Is a | genotype |
| of | rs79556279 |
| Gene | |
| Chromosome | 6 |
| Position | 31,362,069 |
| mentioned | by |
| Magnitude | 4.11 |
| Repute | Bad |
| 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 |
HLA-B*51 the primary risk in Behçet's disease and rs79556279=T has the strongest association of any SNP in the HLA-B region. [PMID 24876276]
