rs2200733, None

N. diseases: 12
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
0.730 GeneticVariation GWASCAT Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study. 26708676 2016
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
0.730 GeneticVariation BEFREE Our results show that the SNP rs2200733</span> and r</span>s6843082 have no significant associations with IS in additive, dominant, recessive, and allelic models (all p > 0.050). 25711478 2015
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
0.730 GeneticVariation BEFREE No significant association was found between rs2200733 and ischemic stroke. 19707791 2009
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
0.730 GeneticVariation BEFREE We discovered that variants previously shown to associate with atrial fibrillation (AF), rs2200733 and rs10033464, significantly associated with IS, with the strongest risk for CES. 18991354 2008