rs2200733, None

N. diseases: 12
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cardioembolic stroke
CUI: C1531624
Disease: Cardioembolic stroke
0.030 GeneticVariation BEFREE Subsequently subgroup analysis indicated that both rs2200733 and rs10033464 conferred increased risk for cardioembolic stroke (CE stroke) (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
Cardioembolic stroke
CUI: C1531624
Disease: Cardioembolic stroke
0.030 GeneticVariation BEFREE The rs2200733 variant on chromosome 4q25 is a risk factor for cardioembolic stroke related to atrial fibrillation in Polish patients. 21574119 2011
Cardioembolic stroke
CUI: C1531624
Disease: Cardioembolic stroke
0.030 GeneticVariation BEFREE In the Icelandic samples and the two replication sets combined, rs2200733 associated significantly with cardioembolic stroke (CES) (odds ratio [OR], 1.54; p = 8.05 x 10(-9)). 18991354 2008