rs2066844(T;T)
From SNPedia
| Significance unclear; possibly higher risk for Crohn's disease |
| Is a | genotype |
| of | rs2066844 |
| Gene | NOD2 |
| Chromosome | 16 |
| Position | 50,712,015 |
| mentioned | by |
| Magnitude | 3.1 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| (C;T) | 2 | Significance is unclear, but possibly, ~2x higher risk for Crohn's disease |
| (T;T) | 3.1 | Significance unclear; possibly higher risk for Crohn's disease |
