Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2200733
rs2200733 		0.820 GeneticVariation BEFREE Subsequently subgroup analysis indicated that both rs2200733 and rs10033464 conferred increased risk for cardioembolic stroke (CE str</span>oke) (for rs2200733, OR 1.38, 95 % CI 1.26-1.51; for rs10033464, OR 1.14, 95 % CI 1.02-1.26), while rs2200733 was marginal associated with non-CE stroke (OR 1.09, 95 % CI 1.02-1.16). our results demonstrated that two SNPs (rs2200733 and rs1003346) on chromosome 4q25 were limited to the stroke of cardioembolic etiology. 24065534

2013
dbSNP: rs2200733
rs2200733 		0.820 GeneticVariation GWASDB Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. 22306652

2012
dbSNP: rs2200733
rs2200733 		0.820 GeneticVariation BEFREE The SNP rs2200733 on chromosome 4q25 is a risk factor for CE stroke related to AF only. 21574119

2011
dbSNP: rs2200733
rs2200733 		T 0.820 GeneticVariation GWASDB Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. 18991354

2008
dbSNP: rs2200733
rs2200733 		T 0.820 GeneticVariation GWASCAT Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. 18991354

2008