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Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.

PMID 26999117 | PMCID PMC4813250 | DOI 10.3390/ijms17030395 · International journal of molecular sciences · 2016 · 8 validated mentions
TypeEntitySource evidenceConfidenceExtractor
variantrs4977574“Association analysis of 12 SNPs indicated a significant difference in the genotype distribution for four SNPs between cases and controls (rs564398 p = 0.0315, χ² = 4.6, odds ratio (OD) = 1.5; rs4977574 p = 0.0336, χ² = 4.5, OD = 1.4; rs2891168 p = 1.85 × 10 - 10, χ² = 40.6, OD = 2.1 and rs1333042 p = 5.14 × 10 - 9, χ² = 34.1, OD = 2.2).”0.90hgvs_regex_v1
geneCDKN2B-AS1“Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.”0.98hgnc_dict_v1
phenotypecoronary artery disease“Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.”0.98phenotype_alias_lexicon_v2
phenotypemyocardial infarction“Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.”0.98phenotype_alias_lexicon_v2