Barely Significant
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Genetic variant rs1205 is associated with COVID-19 outcomes: The Strong Heart Study and Strong Heart Family Study.

PLoS One · 2024 · PMC11045144 · PMID 38662664

1
hedged sentence
0.0490
closest p · 1.0× alpha
0.0490
boldest claim

The sentences

nominally significantp = 0.049actually significant
Among 21 candidate variants including genes in the interferon response pathway, APOE , TMPRSS2 , TLR3 , the HLA complex and the ABO blood group, only rs1205, a 3’ untranslated region variant in the CRP gene, showed nominally significant association in T-dominant model analyses (odds ratio 1.859, 95%CI 1.001–3.453, p = 0.049) after adjustment for age, sex, center, body mass index, and a history of cardiovascular disease.

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