Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12425791
rs12425791
0.890 GeneticVariation BEFREE These findings indicate that rs12425791 G>A polymorphism may be a low-penetrance susceptibility marker of stroke in Asian populations and further studies are warranted to verify this association. 26312640

2016

dbSNP: rs12425791
rs12425791
0.890 GeneticVariation BEFREE A recent genome-wide association study (GWAS) identified two common polymorphisms (rs12425791 and rs11833579) on chromosome 12p13 that confer risk to stroke, particularly for large artery atherosclerotic (LAA) stroke. 26687183

2016

dbSNP: rs12425791
rs12425791
0.890 GeneticVariation BEFREE These results suggested that the rs12425791 and rs11833579 polymorphisms on Chromosome 12p13 may be associated with the risk of LAA stroke and might be used as candidate biomarkers for LAA stroke susceptibility. 26145198

2015

dbSNP: rs12425791
rs12425791
0.890 GeneticVariation BEFREE rs12425791 and rs11833579 were not associated with age of stroke onset (P = 0.786 and 0.340, respectively). 24995625

2014

dbSNP: rs12425791
rs12425791
0.890 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
0.890 GeneticVariation BEFREE In 2009, a GWAS has confirmed that rs11833579 and rs12425791 near the NINJ2 gene could increase the stroke and ischemic stroke (IS) risk. 22795341

2012

dbSNP: rs12425791
rs12425791
0.890 GeneticVariation BEFREE Recent genome-wide association studies (GWAS) have identified two key SNPs (rs11833579 and rs12425791) on chromosome 12p13 that were significantly associated with stroke in Caucasians. 22938733

2012

dbSNP: rs12425791
rs12425791
0.890 GeneticVariation BEFREE Recent genome-wide association (GWA) studies have identified two intergenic single nucleotide polymorphisms (SNPs) (rs11833579 and rs12425791) on chromosome 12p13 and within 11 kb of the NINJ2 gene that were significantly associated with stroke in Caucasians. 21376321

2011

dbSNP: rs12425791
rs12425791
0.890 GeneticVariation BEFREE Our data suggest that rs12425791 on chromosome 12p13 is a genetic marker for atherothrombotic stroke in multiethnic population. 20448654

2010

dbSNP: rs12425791
rs12425791
A 0.890 GeneticVariation GWASDB Genomewide association studies of stroke. 19369658

2009

dbSNP: rs12425791
rs12425791
A 0.890 GeneticVariation GWASCAT Genomewide association studies of stroke. 19369658

2009