Barely Significant
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Rare variant genetic landscape of familial chylomicronemia syndrome (FCS) in the United Kingdom.

Genet Med Open · 2025 · PMC12409453 · PMID 40919303

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hedged sentence
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closest p · 2.0× alpha
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boldest claim

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a nonsignificant trendP < .1so close (0.05 < p ≤ 0.1)
The mean age at genetic testing was younger in females (40.2 [16.3] vs 44.0 [14.3] years, P < .001), and there was a nonsignificant trend of genetic diagnosis of FCS at an earlier age in females (32.2 [17.5] vs 38.1 [19.1] years, P < .1; P = .09).

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