Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2228262
rs2228262
0.040 GeneticVariation BEFREE Our data suggests that the presence of thrombospondin-1 (rs2228262) and thrombospondin-2 (rs8089) variants need not be considered a risk for coronary artery disease or myocardial infarction among South Indians. 21762961

2011

dbSNP: rs2228262
rs2228262
0.040 GeneticVariation BEFREE In a large case-control study of 1425 individuals who survived a myocardial infarction prior to age 45, the N700S polymorphism was a significant risk factor for myocardial infarction in both homozygous (odds ratio [OR] 1.9, 95% confidence interval [CI] 1.1-3.3, P = .01) and heterozygous carriers of the S700 allele (OR 1.4, 95% CI 1.1-3.3, P = .01). 16684956

2006

dbSNP: rs2228262
rs2228262
0.040 GeneticVariation BEFREE Our study suggested that the TSP-1 N700S polymorphism was rare and unrelated to MI in the Chinese Han population. 15140581

2004

dbSNP: rs2228262
rs2228262
0.040 GeneticVariation BEFREE Recently, polymorphisms in thrombospondin (THBS) genes coding for THBS-1 (N700S), THBS-2 (T>G substitution in 3'-untranslated region), and THBS-4 (A387P) genes were proposed to modulate the risk of premature coronary artery disease (CAD) or myocardial infarction (MI). 12482844

2002