Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800469
rs1800469
0.020 GeneticVariation BEFREE In the subset analysis by the type of MI, significantly elevated risk of MI</span> was associated with the homozygote TT and heterozygote C/T in no-AMI subjects, when compared with the CC homozygote carriers (OR = 1.12, 95% CI:1.02-1.23).Our meta-analysis shows that the polymorphism with homozygote TT and heterozygote C/T of TGF-β 509C/T (rs1800469) is significantly associated with the increased risk of MI. 31261499

2019

dbSNP: rs1800469
rs1800469
0.020 GeneticVariation BEFREE We investigated whether the -509C/T (rs1800469), 868T/C (rs1982073), 913G/C (rs1800471), and 11929C/T (rs1800472) polymorphisms of TGFB1 are associated with myocardial infarction. 16543493

2006

dbSNP: rs1800470
rs1800470
0.020 GeneticVariation BEFREE No association between the TGF-beta1 polymorphisms and myocardial infarction was observed; however, the -509 C/T and codon 10 Leu/Pro polymorphisms were associated with the risk of stroke. 17023672

2006

dbSNP: rs1800471
rs1800471
0.020 GeneticVariation BEFREE We therefore investigated 5 polymorphisms in the TGF-beta1 gene (-800 G/A, -509 C/T, codon 10 Leu/Pro, codon 25 Arg/Pro, and codon 263 Thr/Ile) in relation to the risk of myocardial infarction and stroke in a population-based study. 17023672

2006

dbSNP: rs1800471
rs1800471
0.020 GeneticVariation BEFREE We investigated whether the -509C/T (rs1800469), 868T/C (rs1982073), 913G/C (rs1800471), and 11929C/T (rs1800472) polymorphisms of TGFB1 are associated with myocardial infarction. 16543493

2006

dbSNP: rs1800472
rs1800472
0.020 GeneticVariation BEFREE We investigated whether the -509C/T (rs1800469), 868T/C (rs1982073), 913G/C (rs1800471), and 11929C/T (rs1800472) polymorphisms of TGFB1 are associated with myocardial infarction. 16543493

2006

dbSNP: rs1800472
rs1800472
0.020 GeneticVariation BEFREE We therefore investigated 5 polymorphisms in the TGF-beta1 gene (-800 G/A, -509 C/T, codon 10 Leu/Pro, codon 25 Arg/Pro, and codon 263 Thr/Ile) in relation to the risk of myocardial infarction and stroke in a population-based study. 17023672

2006

dbSNP: rs1800470
rs1800470
0.020 GeneticVariation BEFREE In humans, a T-->C transition at nucleotide 29 in the region encoding the signal peptide sequence of the transforming growth factor (TGF)-beta(1), which results in a Leu-->Pro substitution at codon 10, has been associated with myocardial infarction. 12649573

2003

dbSNP: rs1982073
rs1982073
0.010 GeneticVariation BEFREE We investigated whether the -509C/T (rs1800469), 868T/C (rs1982073), 913G/C (rs1800471), and 11929C/T (rs1800472) polymorphisms of TGFB1 are associated with myocardial infarction. 16543493

2006