Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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0.080 | GeneticVariation | BEFREE | Similarly, a higher risk of IS was also observed in the combined genotypes of the rs10757278 AG/GG and rs9333358 AG/GG (95% CI: 1.34-2.83, P < 0.001). | 31810024 | 2020 |
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0.080 | GeneticVariation | BEFREE | However, we are unable to identify any association between rs10757278 and IS. | 31055994 | 2019 |
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0.080 | GeneticVariation | BEFREE | Additionally, rs1075</span>7278 polymorphism was also significantly correlated with an increased risk of IS in Caucasians. | 30962266 | 2019 |
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0.080 | GeneticVariation | BEFREE | There were no statistically significant differences in the distribution of genotypes and alleles of the rs10757278 polymorphism between groups of children with arterial ischemic stroke and controls. | 28778720 | 2017 |
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|
0.080 | GeneticVariation | BEFREE | This study is the first one to demonstrate that the rs10757278-GG genotype, the rs1537378-C allele, and rs1333047-TT genotype are associated with IS in Chinese Han populations. | 25724239 | 2015 |
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0.080 | GeneticVariation | BEFREE | Overall, the summary odds ratio of IS was 1.11 (95% CI: 1.07-1.15, P<10(-5)) for rs10757278. | 24625579 | 2014 |
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0.080 | GeneticVariation | BEFREE | ANCOVA and multivariable logistic regression modeling were performed to determine independent genetic associations between the key chromosome 9p21.3 SNP, rs10757278, and ischemic stroke by comparing allele frequencies between 229 patients with stroke or TIA and an equal number of matched nonstroke controls, adjusting for other risk factors. | 21088391 | 2011 |
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0.080 | GeneticVariation | BEFREE | Meta-analysis confirmed that both rs1537378 and rs10757278 are risk factors for ischemic stroke (ORs, 1.09 [P=0.0014] and 1.11 [P=0.001], respectively). | 20395606 | 2010 |