Association testing of each of the five SNPs genotyped in the <i>ACCN1</i>.

nExpected frequency of pseudocases carrying the variant allele. oExpected frequency of pseudocontrols carrying the variant allele. pThe first number is the unadjusted p-value for the null hypothesis of no association of the SNP, based on the Z statistic for the 2×2 table comparing the two alleles of the SNP. The second number, in brackets, is the corresponding adjusted version of the p-value, calculated through the LOCAL test procedure described in the Statistical analysis section, to correct for the five-fold multiplicity. qThe first number is the unadjusted p-value for the null hypothesis of no association of the SNP, based on an unconditional weighted logistic regression. The second number, in brackets, is the corresponding adjusted version of the p-value, calculated through the REG test procedure described in the Statistical analysis section, to correct for the five-fold multiplicity. The symbol “N.S.” stands for “statistically non significant”.