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The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants

Table 8

Significant CD phenotype associations of rs2066843 and rs2076756 as shown in Tables 5, 6 and 7 stratified for the presence (NOD2+) or absence (NOD2-) of the three CD-associated NOD2 mutations p.Arg702Trp (rs2066844), p.Gly908Arg (rs2066847), and p.Leu1007fsX1008 (rs2066847).

Table 8

doi: https://doi.org/10.1371/journal.pone.0014466.t008