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. 2012 Jan 12;7(1):e29872. doi: 10.1371/journal.pone.0029872

Table 2. Allelic analyses of CD1D and CD1B variants in the CCALD and AMN patients.

SNP (dbSNP31) gene MAF MAF AMN MAF CCALD χ2 P value empirical P valueb Odds ratio [CI95%]
rs859008 CD1D 0.09 0.14 0.06 5.99 0.018a 0.020 0.36 [0.16 ; 0.84]
rs859009 0.09 0.15 0.06 7.13 0.010a 0.010 0.34 [0.15 ; 0.77]
rs859013 0.09 0.14 0.05 6.9 0.014a 0.016 0.33 [0.14 ; 0.78]
rs422236 0.41 0.42 0.40 0.12 0.73 - 0.92 [0.56 ; 1.50]
rs11583390 CD1B 0.03 0.03 0.03 - - - -
rs16840096 0.11 0.16 0.09 3.22 0.073 0.118 0.51 [0.24 ; 1.08]
rs3176842 0.17 0.17 0.16 0.05 0.82 - 0.93 [0.49 ; 1.78]
rs35841099 0.004 0.01 0 - - - -
rs962879 0.12 0.17 0.09 3.64 0.056 0.106 0.49 [0.23 ; 1.31]
rs62642468 0.03 0.05 0.02 - - - -
a

: The Fisher's exact test was used for SNP with a Minor Allele Frequency (MAF)<0.10.

b

: Permutation-based empirical P value were calculated for SNP showing a trend of association (P value<0.10).