Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12190287
rs12190287
TCF21
0.820 GeneticVariation BEFREE Functional rs12190287</span> polymorphisms located within the 3' untranslated region (3'-UTR) of TCF21 were associated with a risk of coronary heart disease in the European and Eastern populations. 28346832

2017
dbSNP: rs12190287
rs12190287
TCF21
0.820 GeneticVariation BEFREE The lead CHD-associated polymorphism in this region, rs12190287, resides in the 3' untranslated region (3'-UTR) of TCF21, a basic-helix-loop-helix transcription factor, and is predicted to alter the seed binding sequence for miR-224. 24676100

2014
dbSNP: rs12190287
rs12190287
TCF21
0.820 GeneticVariation GWASCAT Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325

2014
dbSNP: rs12190287
rs12190287
TCF21
C 0.820 GeneticVariation GWASDB Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990

2011
dbSNP: rs12190287
rs12190287
TCF21
C 0.820 GeneticVariation GWASCAT Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990

2011