Polymorphic Variants of SCN5A Gene (rs41312433 and rs1805124) Associated with Coronary Artery Affliction in Patients with Severe Arrhythmias.

Genes (Basel) · 2024 · PMC10887539 · PMID 38397190

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closest p

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highly significantp = 6.2 × 10 4a dropped decimal point

Considering the polymorphic variants of SCN5A, rs1805124 (H558G), the G558 allele had similar frequencies in all studies (24.4%, 18.4% and 23.4%, respectively), with a highly significant association with the PR interval value ( p = 6.2 × 10 4 , heterogeneity of p = 0.09).

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