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rs2066847(-;-)

From SNPedia
common in complete genomics
Is agenotype
ofrs2066847
GeneNOD2
Chromosome16
Position50,729,867
Merged fromRs5743293
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 0 common in complete genomics
(-;C) 3 3x higher risk of Crohn's disease
(C;C) 4 35x higher risk for Crohn's disease
(G;G) 0 common on affy axiom data