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. 2017 Dec 11;153(4):523–531. doi: 10.1111/imm.12855

Table 3.

Comparisons between the statistically significant variables (P < 0·05 or P < 0·10) independently associated with the risk of developing symptomatic cytomegalovirus infection in the multiple variable logistic regressions performed in the complete case database (n = 98) and after imputing missing values according to the four different imputation methods used (n = 120)

No imputation (P) Method 1 (P) Method 2 (P) Method 3 (P) Method 4 (P) Overall statistically significant
GM3/17 0·99 n.s. 0·8 n.s. 0·4 n.s. 0·6 n.s. 0·7 n.s. 0/5
GM17/17 0·04 1 0·01 1 0·05 2 0·08 2 0·08 2 4/5
GM23−/+ 0·009 1 0·004 1 0·01 1 0·04 1 0·04 1 5/5
GM23+/+ 0·01 1 0·009 1 0·01 1 0·06 2 0·05 2 4/5
KIR2DS2 0·06 2 0·01 1 0·01 1 0·02 1 0·02 1 5/5
KIR2DS5 0·02 1 0·01 1 0·02 1 0·06 2 0·05 2 5/5
HLA‐C2 0·07 2 0·02 1 0·02 1 0·03 1 0·03 1 5/5
HLA‐Bw4T 0·05 2 0·03 1 0·05 2 0·05 2 0·07 2 5/5
Haplotype AA 0·47 n.s. 0·45 n.s. 0·20 n.s. 0·16 n.s. 0·18 n.s. 0/5

We report the following degree of evidence against the null hypothesis: 1statistical significance (P < 0·05); 2weak statistical significance (P < 0·10); n.s., not significant. TThreonine.