Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11596587
rs11596587
HK1
T 0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs12932445
rs12932445
ZFHX3
0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs13143308
rs13143308 		0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs146390073
rs146390073
RGS7
0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs16939239
rs16939239 		A 0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs4444878
rs4444878
F11-AS1
A 0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs4727833
rs4727833
CAV2
G 0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs635634
rs635634 		0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs638704
rs638704 		C 0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs6891174
rs6891174 		0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs74154533
rs74154533
NEURL1
G 0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354

2018
dbSNP: rs2200733
rs2200733 		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
dbSNP: rs2200733
rs2200733 		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
dbSNP: rs2200733
rs2200733 		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
dbSNP: rs152312
rs152312
PDE4D ; PART1
0.020 GeneticVariation BEFREE Our findings demonstrated an association between cardioembolic stroke and phosphodiesterase 4D single nucleotide polymorphisms rs152312 and 45. 21989204

2011
dbSNP: rs152312
rs152312
PDE4D ; PART1
0.020 GeneticVariation BEFREE The rs152312 SNP was associated with cardioembolic stroke among whites after multiple comparison corrections. 16373644

2006
dbSNP: rs2273235
rs2273235
NDST1
0.010 GeneticVariation BEFREE Similar results were found for m<sup>6</sup>A-SNP rs2273235 in the <i>NDST1</i> gene which was associated with cardioembolic stroke (<i>P</i> = 8.47 × 10<sup>-3</sup>). 31156544

2019
dbSNP: rs761740955
rs761740955
FGB
0.010 GeneticVariation BEFREE The β-fibrinogen gene 455G/A polymorphism associated with cardioembolic stroke in atrial fibrillation with low CHA<sub>2</sub>DS<sub>2</sub>-VaSc score. 29235504

2017
dbSNP: rs1217691063
rs1217691063
MTHFR
0.010 GeneticVariation BEFREE MTHFR C677T was associated with magnetic resonance imaging-confirmed lacunar stroke, but not large artery or cardioembolic stroke. 26839351

2016
dbSNP: rs151091899
rs151091899
TRPV3
0.010 GeneticVariation BEFREE The analysis of the TRPV3 gene using polymorphisms in cohort 3 and 4 revealed two polymorphisms associated with cardioembolic stroke in both cohorts, the most significant polymorphism being rs151091899 (p-value: 3.1 × 10<sup>-05</sup>; odds ratio: 5.4) in cohort 3. 27604134

2016
dbSNP: rs1205
rs1205
CRP
0.010 GeneticVariation BEFREE Three polymorphisms, rs1205 (CRP gene), rs1800779, and rs2257073 (NOS3 gene), were associated with cardioembolic stroke (p value <0.05). 26355258

2015
dbSNP: rs1800779
rs1800779
NOS3
0.010 GeneticVariation BEFREE Three polymorphisms, rs1205 (CRP gene), rs1800779, and rs2257073 (NOS3 gene), were associated with cardioembolic stroke (p value <0.05). 26355258

2015
dbSNP: rs20417
rs20417
PTGS2 ; PACERR
0.010 GeneticVariation BEFREE In the Boston cohort, rs20417 polymorphism was associated with increased WMHv among noncardioembolic (P = .037), but not among cardioembolic stroke patients. 25957909

2015
dbSNP: rs2257073
rs2257073
ASB10
0.010 GeneticVariation BEFREE Three polymorphisms, rs1205 (CRP gene), rs1800779, and rs2257073 (NOS3 gene), were associated with cardioembolic stroke (p value <0.05). 26355258

2015
dbSNP: rs1906591
rs1906591 		0.010 GeneticVariation BEFREE Variant rs1906591 on chromosome 4q25 confers increased risk of cardioembolic stroke in Chinese patients. 24932589

2014