Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17465637
rs17465637
0.840 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

dbSNP: rs17465637
rs17465637
0.840 GeneticVariation BEFREE SNPs were genotyped by TaqMan assays and follow-up multivariate logistic regression analysis with incorporation of significant covariates showed significant association with MI for MIA3 SNP rs17465637 (P-adj= 0.0034) and SORT1 SNP rs599839 (P-adj= 0.009). 21463265

2011

dbSNP: rs17465637
rs17465637
0.840 GeneticVariation BEFREE Showing association between rs17465637 and MI, this work was consistent with results from the original detection study and most prior replication studies addressing this issue. 21264445

2011

dbSNP: rs17465637
rs17465637
C 0.840 GeneticVariation GWASCAT Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609

2009

dbSNP: rs17465637
rs17465637
C 0.840 GeneticVariation GWASDB Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609

2009

dbSNP: rs17465637
rs17465637
0.840 GeneticVariation BEFREE Although the underlying mechanisms are not clearly understood, the previously reported association between the 2 SNPs (rs1333049 and rs17465637) and MI was reproduced in this Japanese sample. 18654002

2008