Logistic regression analysis to look for effect of childs' alleles at ABCA4 and COL2A1 on clinical outcome in children in the EMSCOT cohort who became infected in utero.

SNP = single nucleotide polymorphism; OR = odds ratio; CI = 95% confidence intervals; P = probability. Data shown only markers were PTable 4), P��0.05 is shown in bold. No associations were observed at VMD2 or TIMP3 for any phenotype (data not shown). All analyses for the EMSCOT study were adjusted for country of birth, trimester of seroconversion, and country of origin of grandparents as a surrogate for ethnicity.aDetails of allele frequencies provided in Table S1.bPhenotypes of children infected in utero from mothers infected during pregnancy. Table S8 provides full details of the numbers of children carrying each genotype for each phenotypic group.