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. 2012 Sep 1;6(4):413–416. doi: 10.4161/pri.21773

Table 1. Genotype and allele frequencies of the 1368 and 129 PRNP polymorphisms among sCJD patients and controls.

 
sCJD n (%)
Controls n (%)
OR
95% CI
p value*
1368 genotype          
TT
21(45.6)
35 (25.4)
reference
 
 
TC
16 (34.8)
70 (50.7)
0.381
0.177–0.820
0.018
CC 9 (19.6) 33 (23.9) 0.455 0.182–1.134 0.121
1368 allele          
T
58 (63.0)
140 (50.7)
reference
 
 
C 34 (37.0) 136 (49.3) 0.603 0.372–0.980 0.041
129 genotype          
AA
24 (52.2)
38 (27.5)
3.411
1.512–7.758
0.0013
AG
15 (32.6)
81 (58.7)
reference
 
 
GG 7 (15.2) 19 (13.8) 1.989 0.630–6.177 0.248
129 allele          
A
63 (68.5)
157 (56.9)
reference
 
 
G 29 (31.5) 119 (43.1) 1.647 0.971–2.802 0.051
Genotype
1368–129
         
TT-AA
3 (6.5)
8 (5.8)
0.580
0.126–2.672
0.713
TC-AA
13 (28.2)
11 (8)
1.826
0.605–5.512
0.403
CC-AA
8 (17.4)
19 (13.8)
0.651
0.212–1.997
0.573
TT-AG
11 (24.0)
17 (12.3)
reference
 
 
TC-AG
3 (6.5)
50 (36.2)
0.093
0.023–0.372
0.0003
CC-AG
1 (2.2)
14 (10.1)
0.110
0.013–0.963
0.033
TT-GG
7 (15.2)
10(7.2)
1.082
0.317–3.694
1.000
TC-GG 0 9 (6.5)     0.036
*

Two-tailed Fisher’s exact test; OR, odds ratio; CI, confidence interval.