rs116488202(C;C)
From SNPedia
| common in complete genomics |
| Is a | genotype |
| of | rs116488202 |
| Gene | |
| Chromosome | 6 |
| Position | 31,377,139 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| (C;T) | 3 | likely to carry one HLA-B27 allele, possible risk for B27 Syndromes. |
| (T;T) | 3 | likely to carry two HLA-B27 alleles, possible risk for B27 Syndromes. |
