Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs2066843(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs2066843
GeneNOD2
Chromosome16
Position50,711,288
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(T;T) 2 4.09x higher risk for Crohn's disease