rs2066844(C;T)
From SNPedia
Significance is unclear, but possibly, ~2x higher risk for Crohn's disease |
Is a | genotype |
of | rs2066844 |
Gene | NOD2 |
Chromosome | 16 |
Position | 50,712,015 |
mentioned | by |
Magnitude | 2 |
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 |