<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zheng PF</submitter><funding>National Natural Science Foundation of China</funding><pagination>13010</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7400760</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(1)</volume><pubmed_abstract>This research aimed to assess the associations of 7 parkin RBR E3 ubiquitin protein ligase (PRKN) and 4 parkin coregulated gene (PACRG) single-nucleotide polymorphisms (SNPs), their haplotypes, gene-gene (G × G) and gene-environment (G × E) interactions with hyperlipidaemia in the Chinese Maonan minority. The genotypes of the 11 SNPs in 912 normal and 736 hyperlipidaemic subjects were detected with next-generation sequencing technology. The genotypic and allelic frequencies of the rs1105056, rs10755582, rs2155510, rs9365344, rs11966842, rs6904305 and rs11966948 SNPs were different between the normal and hyperlipidaemic groups (P &lt; 0.05-0.001). Correlations between the above 7 SNPs and blood lipid levels were also observed (P &lt; 0.0045-0.001, P &lt; 0.0045 was considered statistically significa</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Associations of PRKN-PACRG SNPs and G × G and G × E interactions with the risk of hyperlipidaemia.</pubmed_title><pmcid>PMC7400760</pmcid><funding_grant_id>81460169</funding_grant_id><pubmed_authors>Liu CX</pubmed_authors><pubmed_authors>Yin RX</pubmed_authors><pubmed_authors>Deng GX</pubmed_authors><pubmed_authors>Wei BL</pubmed_authors><pubmed_authors>Guan YZ</pubmed_authors><pubmed_authors>Zheng PF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Associations of PRKN-PACRG SNPs and G × G and G × E interactions with the risk of hyperlipidaemia.</name><description>This research aimed to assess the associations of 7 parkin RBR E3 ubiquitin protein ligase (PRKN) and 4 parkin coregulated gene (PACRG) single-nucleotide polymorphisms (SNPs), their haplotypes, gene-gene (G × G) and gene-environment (G × E) interactions with hyperlipidaemia in the Chinese Maonan minority. The genotypes of the 11 SNPs in 912 normal and 736 hyperlipidaemic subjects were detected with next-generation sequencing technology. The genotypic and allelic frequencies of the rs1105056, rs10755582, rs2155510, rs9365344, rs11966842, rs6904305 and rs11966948 SNPs were different between the normal and hyperlipidaemic groups (P &lt; 0.05-0.001). Correlations between the above 7 SNPs and blood lipid levels were also observed (P &lt; 0.0045-0.001, P &lt; 0.0045 was considered statistically significa</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Aug</publication><modification>2026-05-02T06:33:43.166Z</modification><creation>2020-11-19T16:53:59Z</creation></dates><accession>S-EPMC7400760</accession><cross_references><pubmed>32747620</pubmed><doi>10.1038/s41598-020-68826-1</doi></cross_references></HashMap>