KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures.

ASN Neuro · 2022 · PMC9016559 · PMID 35414199

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hedged sentences

0.0010

closest p · 0.0× alpha

0.1160

boldest claim

The sentences

highly significantp < .001actually significant

We have found that the subgroup of children with CFS shows highly significant difference in the frequencies of the rs2297201 KCC2 genotypes compared to the control group (χ 2 = 14.454; p < .001) ( Table 2 ).

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did not reach statistical significancep = .116not close (p > 0.1)

The genotypes CT and TT of the rs2297201 polymorphism of the KCC2 gene were detected in 6 children (30.0%) in the group of children with epilepsy (EFS) and 14 children (13.08%) in the control group. These difference did not reach statistical significance (χ 2 = 2.471; p = .116) ( Table 2 ).

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