<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Wang H</submitter><pubmed_abstract>&lt;b>Introduction:&lt;/b> Leukocyte immunoglobulin-like receptor A3 (&lt;i>LILRA3&lt;/i>) belongs to the LILR family with unique feature of a 6.7-kb deletion variation among individuals. Frequencies of the 6.7-kb deletion vary widely across populations, but so far it has not been carefully investigated among Han Chinese subpopulations. Furthermore, we previously identified the non-deleted (functional) &lt;i>LILRA3&lt;/i> as a novel genetic risk for multiple autoimmune diseases. The current study aimed to investigate (i) whether frequencies of the &lt;i>LILRA3&lt;/i> 6.7-kb deletion differ within Han Chinese subpopulations and (ii) whether the functional &lt;i>LILRA3&lt;/i> is a novel genetic risk for ankylosing spondylitis (AS). &lt;b>Methods:&lt;/b> The &lt;i>LILRA3&lt;/i> 6.7-kb deletion was genotyped in two independent cohorts</pubmed_abstract><journal>Frontiers in genetics</journal><pagination>869</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6760026</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Frequencies of the &lt;i>LILRA3&lt;/i> 6.7-kb Deletion Are Highly Differentiated Among Han Chinese Subpopulations and Involved in Ankylosing Spondylitis Predisposition.</pubmed_title><pmcid>PMC6760026</pmcid><pubmed_authors>Lv J</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Guo J</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Cai Y</pubmed_authors><pubmed_authors>Zhou G</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Ye H</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Frequencies of the &lt;i>LILRA3&lt;/i> 6.7-kb Deletion Are Highly Differentiated Among Han Chinese Subpopulations and Involved in Ankylosing Spondylitis Predisposition.</name><description>&lt;b>Introduction:&lt;/b> Leukocyte immunoglobulin-like receptor A3 (&lt;i>LILRA3&lt;/i>) belongs to the LILR family with unique feature of a 6.7-kb deletion variation among individuals. Frequencies of the 6.7-kb deletion vary widely across populations, but so far it has not been carefully investigated among Han Chinese subpopulations. Furthermore, we previously identified the non-deleted (functional) &lt;i>LILRA3&lt;/i> as a novel genetic risk for multiple autoimmune diseases. The current study aimed to investigate (i) whether frequencies of the &lt;i>LILRA3&lt;/i> 6.7-kb deletion differ within Han Chinese subpopulations and (ii) whether the functional &lt;i>LILRA3&lt;/i> is a novel genetic risk for ankylosing spondylitis (AS). &lt;b>Methods:&lt;/b> The &lt;i>LILRA3&lt;/i> 6.7-kb deletion was genotyped in two independent cohorts</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-05-04T19:01:55.946Z</modification><creation>2019-10-30T08:17:31Z</creation></dates><accession>S-EPMC6760026</accession><cross_references><pubmed>31620171</pubmed><doi>10.3389/fgene.2019.00869</doi></cross_references></HashMap>