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 |
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 |
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 |
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 |
rs12425791
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The single-nucleotide polymorphism rs12425791 does not confer a substantial risk for ischemic stroke in Chinese populations.
|
23270316 |
2013 |
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 |
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 |
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 |
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 |
rs12425791
|
|
|
0.100 |
GeneticVariation |
BEFREE |
the single-nucleotide polymorphism rs12425791 does not confer a substantial risk for ischemic stroke in our population.
|
21148441 |
2011 |
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 |
rs12425791
|
|
|
0.100 |
GeneticVariation |
BEFREE |
However, the association between rs12425791 and IS was insignificant in Chinese Han population.
|
21832970 |
2011 |
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 |
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 |