rs3819299(C;C)
From SNPedia
| likely to carry two HLA-B27 alleles, possible risk for B27 Syndromes. |
| Is a | genotype |
| of | rs3819299 |
| Gene | HLA-B |
| Chromosome | 6 |
| Position | 31,354,590 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;C) | 3 | likely to carry one HLA-B27 allele, possible risk for B27 Syndromes. |
| (C;C) | 3 | likely to carry two HLA-B27 alleles, possible risk for B27 Syndromes. |
See details at: HLA-B27 Syndromes.
Not all allelles of HLA-B27 are at risk for B27 Syndromes, please check the HLA-B27 page for details.
