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Table 1 Summary of CTSD rs17571:C>T SNP genotyping and statistical analysis for vCJD patients and UK controls [29].

From: Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob disease

CTSD rs17571: C>T SNP vCJD n (%) Controls n (%) Fisher's exact test p-value OR (95% CI); p-value
CC 89 (80.9) 648 (84.5) 0.023 OR TT/CC = 10.92 (1.80–66.26); 0.009
CT 18 (16.4) 117 (15.3)   OR TT/CT = 9.75 (1.52–62.47); 0.016
TT 3 (2.7) 2 (0.3)   
C 196 (89.1) 1413 (92.1) 0.13 OR T/C = 1.43 (0.90–2.27); 0.11
T 24 (10.9) 121 (7.9)