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One of the main clinical manifestations of <jats:styled-content style=\"fixed-case\">PCM<\/jats:styled-content> is the presence of oral lesions with the presence of epithelioid granulomas. In this work, we aimed to evaluate the frequency of <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s in the <jats:italic><jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content>\u2010<\/jats:italic>\u03b1, <jats:italic><jats:styled-content style=\"fixed-case\">JAK<\/jats:styled-content>1<\/jats:italic>,<jats:italic> <jats:styled-content style=\"fixed-case\">VDR<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> DC<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">SIGN<\/jats:styled-content><\/jats:italic> and <jats:italic>Fc<\/jats:italic>\u03b3<jats:italic><jats:styled-content style=\"fixed-case\">RII<\/jats:styled-content>a<\/jats:italic> genes in patients with chronic <jats:styled-content style=\"fixed-case\">PCM<\/jats:styled-content> and verify possible association of these <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s with the organisation pattern of the granulomas in the oral lesions. A total of 66 samples of <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> were obtained from oral lesions biopsies and 106 <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> samples were obtained from healthy individuals. The individuals were genotyped for <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>s in <jats:italic><jats:styled-content style=\"fixed-case\">DC<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">SIGN<\/jats:styled-content><\/jats:italic> (rs4804803), <jats:italic>Fc<\/jats:italic>\u03b3<jats:italic><jats:styled-content style=\"fixed-case\">RII<\/jats:styled-content>a<\/jats:italic> (rs1801274), <jats:italic><jats:styled-content style=\"fixed-case\">JAK<\/jats:styled-content>1<\/jats:italic> (rs11208534), <jats:italic><jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content>\u2010<\/jats:italic>\u03b1 (rs1800629) and <jats:italic><jats:styled-content style=\"fixed-case\">VDR<\/jats:styled-content><\/jats:italic> (rs7975232) by real\u2010time <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content> and allele discrimination method. Granulomas were classified as loose or dense according to the histological pattern. In the <jats:italic><jats:styled-content style=\"fixed-case\">VDR<\/jats:styled-content><\/jats:italic> (rs7975232), the <jats:styled-content style=\"fixed-case\">CC<\/jats:styled-content> genotype (<jats:italic>P<\/jats:italic>\u00a0&lt;\u00a00.001, <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\u00a0=\u00a05.94, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\u00a0=\u00a02.07\u201017.05), and the C allele (<jats:italic>P<\/jats:italic>\u00a0=\u00a00.027, <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\u00a0=\u00a02.71, 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\u00a0=\u00a01.07\u20106.86), as well as the <jats:styled-content style=\"fixed-case\">GG<\/jats:styled-content> genotype in <jats:italic><jats:styled-content style=\"fixed-case\">DC<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">SIGN<\/jats:styled-content><\/jats:italic> (rs4804803) (<jats:italic>P<\/jats:italic>\u00a0=\u00a00.032, OR: 3.76, 95%, <jats:italic>I<\/jats:italic>\u00a0=\u00a01.06\u201013.38) are associated with an increased risk of oral <jats:styled-content style=\"fixed-case\">PCM<\/jats:styled-content>. Our data indicate that <jats:italic><jats:styled-content style=\"fixed-case\">VDR<\/jats:styled-content><\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">DC<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">SIGN<\/jats:styled-content><\/jats:italic> genetics variations are related to the susceptibility of oral <jats:styled-content style=\"fixed-case\">PCM<\/jats:styled-content> in the group of patients analysed.<\/jats:p>","DOI":"10.1111\/myc.12866","type":"journal-article","created":{"date-parts":[[2018,10,27]],"date-time":"2018-10-27T05:02:37Z","timestamp":1540616557000},"page":"186-192","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":7,"title":["<i><scp>DC<\/scp>\u2010<scp>SIGN<\/scp><\/i> and <i><scp>VDR<\/scp><\/i> polymorphisms are associated with chronic form of paracoccidioidomycosis with oral 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