Skip to main content

Table 1 Estimated frequencies of NOD2 genotypes in probands and FDRs, and estimated FDRs' probability of developing CD.

From: Trial Protocol: Communicating DNA-based risk assessments for Crohn's disease: a randomised controlled trial assessing impact upon stopping smoking

 

NOD2 mutation negative

NOD2 mutation heterozygous

NOD2 mutation homozygous

Frequency of NOD2 genotype in CD probands

65%

27%

8%

Frequency of NOD2 genotype among FDRs

75%

22%

3%

Frequency of NOD2 genotype in controls

87%

12%

1%

Risk to FDRs of developing CD conferred by genotype

2%

4%

15%