Barely Significant
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Genetic loci associated with heart rate variability and their effects on cardiac disease risk.

Nat Commun · 2017 · PMC5474732 · PMID 28613276

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closest p · 0.0× alpha
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The sentences

highly significantP =3.45 × 10 −7actually significant
These two highly significant SNPs (rs10842383 near LINC00477 , P =3.45 × 10 −7 and rs2680344 in HCN4 , P =4.34 × 10 −7 ( Supplementary Table 12 ) had large opposite effects on atrial fibrillation, while both decreased HRV.

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