Barely Significant
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Genetic susceptibility to multiple sclerosis: interactions between conserved extended haplotypes of the MHC and other susceptibility regions.

BMC Med Genomics · 2021 · PMC8272333 · PMID 34246256

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hedged sentence
0.0000
closest p · 0.0× alpha
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boldest claim

The sentences

highly significantp < 10 −10actually significant
Moreover, assessing, collectively, only those ( H +)-carrying CEHs that had a single representation in the WTCCC, the disease association is still highly significant and of similar magnitude to other ( H +)-carrying CEHs (i.e., OR = 3.0; CI = 2.7 − 3.4; p < 10 −10 ).

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