Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5629
rs5629
PTGIS
0.030 GeneticVariation BEFREE The present results indicate that MI is associated with the CC genotype of rs5629 in the human CYP8A1 gene. 19147528

2009
dbSNP: rs5629
rs5629
PTGIS
0.030 GeneticVariation BEFREE Previously, we discovered 3 polymorphisms in the prostacyclin synthase (PGIS) gene: 1) T-192G, in the 5-flanking region, a novel single-nucleotide polymorphism (SNP) that is not associated with essential hypertension (EH); 2) a variable number of tandem repeat (VNTR) polymorphism, 6 nucleotides upstream from the ATG start codon, that is associated with risk of cerebral infarction; and 3) C1117A, in exon 8, an SNP that does not cause an amino acid change in codon 373, and that is associated with risk of myocardial infarction (MI). 12924623

2003
dbSNP: rs5629
rs5629
PTGIS
0.030 GeneticVariation BEFREE We conclude that the C1117A polymorphism in exon 8 is associated with risk for MI and may be a genetic marker of MI in Japanese persons. 12040339

2002