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rs2066844(C;C)

From SNPedia

common in complete genomics
Is agenotype
ofrs2066844
GeneNOD2
Chromosome16
Position50,712,015
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in complete genomics
(C;T) 3 3x higher risk for Crohn's disease
(T;T) 4 ~35x higher risk for Crohn's disease