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. 2017 Jun 19;11(11):1393–1397. doi: 10.1093/ecco-jcc/jjx083

Table 2.

NOD2 genotypes.

Sibling 1 (A) Sibling 2 (B) Mother (C) Father (D)
Pouchitis No Yes No N/A
rs17221417 CC CG CC CG
rs2076756 AA AG AA AG
rs2066844 CC CC CC CC
rs2066847 DD DD DD DD

Crohn’s disease risk allele for each variant is italicized.

DD indicates that the frameshift C insertion was not present.