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Table 1 NOD2/CARD15 SNP8, 12 and 13 in patients with sporadic colorectal cancer (CRC) and (CD) and controls

From: Common NOD2/CARD15 variants are not associated with susceptibility or the clinicopathologic characteristics of sporadic colorectal cancer in Hungarian patients

  R702W (SNP8) G908R (SNP 12) 3020insC (SNP 13)
  CRC n (%) Controls n (%) CRC n (%) controls n (%) CRC n (%) controls n (%)
Wild type 187 (96.4) 194 (97.0) 187 (96.4) 193 (96.5) 180 (92.8) 190 (95.0)
All Carriers 7 (3.6) 6 (3.0) 7 (3.6) 7 (3.5) 14 (7.2) 10 (5.0)
Heterozygous 7 (3.6) 6 (3.0) 7 (3.6) 7 (3.5) 14 (7.2) 10 (5.0)
Allele frequency 7 (1.8) 6 (1.5) 7 (1.8) 7 (1.8) 14 (3.6) 10 (2.5)
P value for carriers 0.78   0.95   0.40  
OR carrier (95%CI) 1.21 (0.39–3.67)   1.03 (0.35–3.00)   1.48 (0.64–3.41)