Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation GWASDB Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project. 21846873

2011
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation BEFREE The T allele of rs2200733 favours larger pulmonary veins and increased number of episodes of AF. 21760908

2011
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation BEFREE The previously reported SNP, rs2200733, was most significantly associated with AF (minor allele odds ratio 1.80, 95% confidence interval 1.50 to 2.15, P=1.2 x 10(-20)) in the discovery sample. 20733104

2010
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation BEFREE The non-coding SNPs rs2200733 and rs10033464 are strongly associated with AF in four cohorts of European descent. 19141561

2009
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation BEFREE Association with postoperative AF were measured and replicated for rs2200733 and rs13143308 in the validation cohort. 20031626

2009
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation GWASCAT A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation GWASDB A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation BEFREE Our results suggest that SNP rs2200733 confers a highly significant risk of AF, but not ischemic stroke, in a more representative Chinese Han population in the mainland China. 19707791

2009
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation BEFREE These results derived from a sample of the Italian population agree with previously reported findings from an Icelandic study, which also found that the minor allele rs2200733 was associated with AF/AFL disease. 18931155

2008
dbSNP: rs2200733
rs2200733 		0.900 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
dbSNP: rs2200733
rs2200733 		T 0.900 GeneticVariation GWASCAT Variants conferring risk of atrial fibrillation on chromosome 4q25. 17603472

2007
dbSNP: rs2200733
rs2200733 		T 0.900 GeneticVariation GWASDB Variants conferring risk of atrial fibrillation on chromosome 4q25. 17603472

2007