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In previous studies, we have shown that genetic polymorphisms and variable expression levels of certain leucocyte receptor complex (<jats:styled-content style=\"fixed-case\">LRC<\/jats:styled-content>) genes were associated with <jats:styled-content style=\"fixed-case\">PF<\/jats:styled-content>. However, the role of the <jats:styled-content style=\"fixed-case\">LRC<\/jats:styled-content> on <jats:styled-content style=\"fixed-case\">PF<\/jats:styled-content> susceptibility remained to be investigated. Here, we analysed 527 tag single nucleotide polymorphisms (<jats:styled-content style=\"fixed-case\">SNPs<\/jats:styled-content>) distributed within the 1\u00b75\u2005Mb <jats:styled-content style=\"fixed-case\">LRC<\/jats:styled-content>. After quality control, a total of 176 <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s were analysed in 229 patients with <jats:styled-content style=\"fixed-case\">PF<\/jats:styled-content> and 194 controls. Three <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s were associated with differential susceptibility to <jats:styled-content style=\"fixed-case\">PF<\/jats:styled-content>. The intergenic variant <jats:italic>rs465169<\/jats:italic> [odds ratio (<jats:styled-content style=\"fixed-case\">OR)\u2005<\/jats:styled-content>=\u20051\u00b750; <jats:italic>P\u2005<\/jats:italic>=\u20050\u00b7004] is located in a region that might regulate several immune\u2010related genes, including <jats:italic><jats:styled-content style=\"fixed-case\">VSTM<\/jats:styled-content>1<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">LILRB<\/jats:styled-content>1\/2<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">LAIR<\/jats:styled-content>1\/2<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">LILRA<\/jats:styled-content>3\/4<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">LENG<\/jats:styled-content>8<\/jats:italic>. The <jats:italic>rs35336528<\/jats:italic> (<jats:styled-content style=\"fixed-case\">OR\u2005<\/jats:styled-content>=\u20053\u00b744; <jats:italic>P\u2005<\/jats:italic>=\u20050\u00b7009) and <jats:italic>rs1865097<\/jats:italic> (<jats:styled-content style=\"fixed-case\">OR\u2005<\/jats:styled-content>=\u20050\u00b757; <jats:italic>P\u2005<\/jats:italic>=\u20050\u00b7005) <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s in <jats:italic><jats:styled-content style=\"fixed-case\">LENG<\/jats:styled-content>8<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">FCAR<\/jats:styled-content><\/jats:italic> genes, respectively, were also associated with <jats:styled-content style=\"fixed-case\">PF<\/jats:styled-content>. Moreover, we found four haplotypes with <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s within the <jats:italic><jats:styled-content style=\"fixed-case\">KIR<\/jats:styled-content>3<jats:styled-content style=\"fixed-case\">DL<\/jats:styled-content>2\/3<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">LAIR<\/jats:styled-content>2<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">LILRB<\/jats:styled-content>1<\/jats:italic> genes associated with <jats:styled-content style=\"fixed-case\">PF<\/jats:styled-content> (<jats:italic>P\u2005<\/jats:italic>&lt;\u20050\u00b705), which corroborate previously reported associations. Thus, our results confirm the importance of the <jats:styled-content style=\"fixed-case\">LRC<\/jats:styled-content> for differential susceptibility to <jats:styled-content style=\"fixed-case\">PF<\/jats:styled-content> and reveal new markers that might influence expression levels of several <jats:styled-content style=\"fixed-case\">LRC<\/jats:styled-content> genes, as well as candidates for further functional studies.<\/jats:p>","DOI":"10.1111\/imm.13003","type":"journal-article","created":{"date-parts":[[2018,9,16]],"date-time":"2018-09-16T06:49:47Z","timestamp":1537080587000},"page":"86-93","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":20,"title":["Screening the full leucocyte receptor complex genomic region revealed associations with pemphigus that might be explained by gene 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