Associations between BMD and CIITA, CLEC16A and IFNG in the OPRA cohort.

*Only associations where p1BMD values are reported as follows: For single SNP analysis (non-carrriers/carriers or common homozygotes/heterozygotes/variant homozygotes); For haplotypes (non-carriers/carriers); For interactions in allelic models (non-carriers of both variant alleles/carriers of both variant alleles); For interactions in genotypic models, values are given for each marker as common homozygotes/heterozygotes/variant homozygotes since no individuals were carriers of both variant alleles.2For rs3087456 * rs4774 genotypic model, p = 0.011.3For rs3087456 * rs4774 genotypic model, p = 0.028.4CLEC16A haplotype 1: rs725613(T)/rs2903692(G)/rs6498169(A).5IFNG haplotype 4: rs2069727(T)/rs2069718(T)/rs2069705(C).