<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(6)</volume><submitter>Pranav Chand R</submitter><pubmed_abstract>In our attempt to comprehensively understand the nature of association of variants at 11q23.3 apolipoprotein gene cluster region, we genotyped a prioritized set of 96 informative SNPs using Fluidigm customized SNP genotyping platform in a sample of 508 coronary artery disease (CAD) cases and 516 controls. We found 12 SNPs as significantly associated with CAD at P &lt;0.05, albeit only four (rs2849165, rs17440396, rs6589566 and rs633389) of these remained significant after Benjamin Hochberg correction. Of the four, while rs6589566 confers risk to CAD, the other three SNPs reduce risk for the disease. Interaction of variants that belong to regulatory genes BUD13 and ZPR1 with APOA5-APOA4 intergenic variants is also observed to significantly increase the risk towards CAD. Further, ROC analysis o</pubmed_abstract><journal>PloS one</journal><pagination>e0153720</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4892567</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.</pubmed_title><pmcid>PMC4892567</pmcid><pubmed_authors>Kumar AS</pubmed_authors><pubmed_authors>Anuj K</pubmed_authors><pubmed_authors>Vishnupriya S</pubmed_authors><pubmed_authors>Mohan Reddy B</pubmed_authors><pubmed_authors>Pranav Chand R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.</name><description>In our attempt to comprehensively understand the nature of association of variants at 11q23.3 apolipoprotein gene cluster region, we genotyped a prioritized set of 96 informative SNPs using Fluidigm customized SNP genotyping platform in a sample of 508 coronary artery disease (CAD) cases and 516 controls. We found 12 SNPs as significantly associated with CAD at P &lt;0.05, albeit only four (rs2849165, rs17440396, rs6589566 and rs633389) of these remained significant after Benjamin Hochberg correction. Of the four, while rs6589566 confers risk to CAD, the other three SNPs reduce risk for the disease. Interaction of variants that belong to regulatory genes BUD13 and ZPR1 with APOA5-APOA4 intergenic variants is also observed to significantly increase the risk towards CAD. Further, ROC analysis o</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2026-05-30T13:48:21.96Z</modification><creation>2019-03-26T22:53:56Z</creation></dates><accession>S-EPMC4892567</accession><cross_references><pubmed>27257688</pubmed><doi>10.1371/journal.pone.0153720</doi></cross_references></HashMap>