rs17465637, MIA3

N. diseases: 11
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.750 GeneticVariation BEFREE In a genome-wide scan, isolated single nucleotide polymorphisms (SNPs), including rs17465637, in the melanoma inhibitory activity 3 gene (MIA3) on chromosome 1 were identified to be associated with coronary artery disease and myocardial infarction (MI). 21264445 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.750 GeneticVariation BEFREE Genome-wide association studies have described an association between MIA3 rs17465637 A/C polymorphisms and coronary artery disease and myocardial infarction. 22577832 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.750 GeneticVariation BEFREE The association between SNP rs1</span>7465637 and CAD became highly significant (P = 4.97 × 10(-5), OR = 1.11). 24125424 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.750 GeneticVariation BEFREE The genetic variants of 1p13 rs599839 and 1q41 rs17465637 SNPs were prominently related to CAD, and the genetic variants of chromosome 1p13 promote the risk of CAD by increased TC and LDLC levels and decreased HDLC levels. 28088267 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.750 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.750 GeneticVariation BEFREE Aim was to estimate the genotypic distribution and risk allele frequencies of 13 Coronary Artery Disease (CAD) risk Single Nucleotide Polymorphisms in loci identified by the CARDIoGRAMplusC4D consortium namely MIA3 rs17465637; 9p21 rs10757274; CXCL12 rs1746048; APOA5 rs662799; APOB rs1042031; LPA rs3798220; LPA 10455872; MRAS rs9818870; LPL rs328; SORT1 rs646776; PCSK9 rs11591147; APOE rs429358; APOE rs7412 in Pakistani PCAD patients and controls. 28705542 2019