Barely Significant
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The 3' end prothrombin gene variants in serbian patients with idiopathic thrombophilia.

Balkan J Med Genet · 2014 · PMC4413441 · PMID 25937797

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Heterozygous carriers of the FII C20068T gene variant were four times more frequent in patients (4.0%) than in controls (1.0%), but this difference did not reach statistical significance (OR = 4.12; 95% CI 0.45–37.57).

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