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Gene\u2010gene interactions between protein\u2010coding genes have been paid great attention, while rare studies refer to the interactions between encoding and noncoding genes. Our research group previously found encoding gene\n                    <jats:styled-content style=\"fixed-case\">PGC<\/jats:styled-content>\n                    polymorphisms could affect the susceptibility to atrophic gastritis (\n                    <jats:styled-content style=\"fixed-case\">AG<\/jats:styled-content>\n                    ) and gastric cancer (\n                    <jats:styled-content style=\"fixed-case\">GC<\/jats:styled-content>\n                    ). Interestingly, several\n                    <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                    s in long noncoding\n                    <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\n                    (lnc\n                    <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\n                    ) genes, just adjacent to\n                    <jats:styled-content style=\"fixed-case\">PGC<\/jats:styled-content>\n                    , were found to be associated with\n                    <jats:styled-content style=\"fixed-case\">AG<\/jats:styled-content>\n                    risk and\n                    <jats:styled-content style=\"fixed-case\">GC<\/jats:styled-content>\n                    prognosis afterward. This study aims to explore the\n                    <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                    interactions between\n                    <jats:styled-content style=\"fixed-case\">PGC<\/jats:styled-content>\n                    and its neighbor lnc\n                    <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\n                    s on the risk of\n                    <jats:styled-content style=\"fixed-case\">AG<\/jats:styled-content>\n                    and\n                    <jats:styled-content style=\"fixed-case\">GC<\/jats:styled-content>\n                    . Genotyping for seven\n                    <jats:styled-content style=\"fixed-case\">PGC SNP<\/jats:styled-content>\n                    s and seven lnc\n                    <jats:styled-content style=\"fixed-case\">RNA SNP<\/jats:styled-content>\n                    s was conducted using Sequenom Mass\n                    <jats:styled-content style=\"fixed-case\">ARRAY<\/jats:styled-content>\n                    platform in a total of 2228 northern Chinese subjects, including 536\n                    <jats:styled-content style=\"fixed-case\">GC<\/jats:styled-content>\n                    cases, 810\n                    <jats:styled-content style=\"fixed-case\">AG<\/jats:styled-content>\n                    cases, and 882 controls. We found 15 pairwise\n                    <jats:styled-content style=\"fixed-case\">PGC<\/jats:styled-content>\n                    \u2010lnc\n                    <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\n                    s\n                    <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                    s had interactions: Five pairs were associated with\n                    <jats:styled-content style=\"fixed-case\">AG<\/jats:styled-content>\n                    risk, and ten pairs were associated with\n                    <jats:styled-content style=\"fixed-case\">GC<\/jats:styled-content>\n                    risk. Moreover, two\n                    <jats:styled-content style=\"fixed-case\">GC<\/jats:styled-content>\n                    \u2010related interactions\n                    <jats:styled-content style=\"fixed-case\">PGC<\/jats:styled-content>\n                    rs6939861 with lnc\u2010C6orf\u2010132\u20101 rs7749023 and rs7747696 survived the Bonferroni correction (\n                    <jats:italic>P<\/jats:italic>\n                    <jats:sub>correction<\/jats:sub>\n                    \u00a0=\u00a00.049 and 0.007, respectively). Several combinations showed obvious epistasis and cumulative effects on disease risk. Some three\u2010way interactions of\n                    <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                    s with smoking and drinking could also be observed. Besides, a few interacting\n                    <jats:styled-content style=\"fixed-case\">SNP<\/jats:styled-content>\n                    s showed correlations with the expression levels of\n                    <jats:styled-content style=\"fixed-case\">PGC<\/jats:styled-content>\n                    protein and related lnc\n                    <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\n                    s in serum. Our study would provide research clues for further screening combination biomarkers uniting both protein\u2010coding and noncoding genes with the potential in prediction of the susceptibility to\n                    <jats:styled-content style=\"fixed-case\">GC<\/jats:styled-content>\n                    and its precursor.\n                  <\/jats:p>","DOI":"10.1002\/cam4.1743","type":"journal-article","created":{"date-parts":[[2018,8,30]],"date-time":"2018-08-30T01:45:00Z","timestamp":1535593500000},"page":"5252-5271","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":8,"title":["<scp>SNP<\/scp>\n                    interactions of\n                    <scp>PGC<\/scp>\n                    with its neighbor lnc\n                    <scp>RNA<\/scp>\n                    s enhance the susceptibility to gastric cancer\/atrophic gastritis and influence the expression of involved 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