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rs2066844(C;T)

From SNPedia
Significance is unclear, but possibly, ~2x higher risk for Crohn's disease
Is agenotype
ofrs2066844
GeneNOD2
Chromosome16
Position50,712,015
mentionedby
Magnitude2
ReputeBad
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