Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE NINJ2 gene rs12425791 confers a susceptible factor for IS, while there is no association between NINJ2 gene rs11833579 and IS. 31258083

2019

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE New evidence from this case-control study and meta-analysis indicates that 12</span>p13 rs12425791</span>/rs1183</span>3579 polymorphisms are associated with ischemic stroke susceptibility in Asian populations. 31679297

2019

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE Our aim of this study was to investigate the association of the rs12425791, rs11833579 and rs12904 in the binding site of miR-200c with the risk of IS. 31077198

2019

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE These findings indicated that rs12425791 and rs11833579 on chromosome 12p13 may be useful biomarkers for predicting the prognosis of patients with the LAA subtype of ischaemic stroke. 24995625

2014

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE The single-nucleotide polymorphism rs12425791 does not confer a substantial risk for ischemic stroke in Chinese populations. 23270316

2013

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE Recent genomewide association studies have revealed an association between two single nucleotide polymorphisms, rs11833579 and rs12425791, and ischemic stroke. 22011019

2012

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE In summary, our meta-analysis suggests that rs12425791 is significantly associated with ischemic stroke in East Asian population but not Chinese Han population, of which A alleles increase the risk of ischemic stroke, whereas no evidence of association was found for rs11833579 in East Asian population as well as Chinese Han population. 22297388

2012

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE This meta-analysis suggest that rs12425791 is relative to ischemic stroke risk under dominant model in Asian population, but not for rs11833579. 22795341

2012

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE This is a precedent study that found genetic variants of rs12425791 and rs11833579 on chromosome 12p13 are independent predictors of stroke-related mortality or stroke recurrence in patients with incident ischemic stroke in Taiwan. 22212150

2012

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE the single-nucleotide polymorphism rs12425791 does not confer a substantial risk for ischemic stroke in our population. 21148441

2011

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE No evidence for association of 12p13 SNPs rs11833579 and rs12425791 within NINJ2 gene with ischemic stroke in Chinese Han population. 21376321

2011

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE However, the association between rs12425791 and IS was insignificant in Chinese Han population. 21832970

2011

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE Recently, a genome-wide association study reported an association between two single nucleotide polymorphisms (SNPs) rs11833579 and rs12425791 near NINJ2 gene and ischemic stroke in Caucasians. 21722921

2011

dbSNP: rs12425791
rs12425791
0.100 GeneticVariation BEFREE Direct genotyping showed that rs12425791 was associated with an increased risk of total (i.e., all types) and ischemic stroke, with hazard ratios of 1.30 (95% confidence interval [CI], 1.19 to 1.42) and 1.33 (95% CI, 1.21 to 1.47), respectively, yielding population attributable risks of 11% and 12% in the discovery cohorts. 19369658

2009