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 | - | - | - | - |
: The Fisher's exact test was used for SNP with a Minor Allele Frequency (MAF)<0.10.
: Permutation-based empirical P value were calculated for SNP showing a trend of association (P value<0.10).