Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1296179669
rs1296179669
MTHFR
0.010 GeneticVariation BEFREE Genotyping was performed using the GenomeLab SNPstream genotyping platform for five IS-relevant SNPs (MMP-9 C1562T, ALOX5AP SG13S114A/T, MTHFR 677 C/T, FGB 455 G/A, and eNOS G298A) in 479 AF patients with CES and 580 age and sex-matched AF patients without CES. 29235504

2017
dbSNP: rs1383209302
rs1383209302
ALOX5AP
0.010 GeneticVariation BEFREE Genotyping was performed using the GenomeLab SNPstream genotyping platform for five IS-relevant SNPs (MMP-9 C1562T, ALOX5AP SG13S114A/T, MTHFR 677 C/T, FGB 455 G/A, and eNOS G298A) in 479 AF patients with CES and 580 age and sex-matched AF patients without CES. 29235504

2017
dbSNP: rs761740955
rs761740955
FGB
0.010 GeneticVariation BEFREE We found for the first time that the A allele of FGB 455 G/A was a risk factor for CES in AF patients, probably by elevating the level of plasma fibrinogen. 29235504

2017
dbSNP: rs1906591
rs1906591 		0.010 GeneticVariation BEFREE The rs1906591 variant is significantly associated with CES in the Chinese Han population, but not with other stroke subtypes. 24932589

2014
dbSNP: rs10033464
rs10033464 		0.010 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 		0.010 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