A Haptoglobin Exon Copy Number Variant Associates With HIV-Associated Neurocognitive Impairment in European and African-Descent Populations.

Front Genet · 2021 · PMC8727522 · PMID 35003209

Europe PMC DOI

hedged sentence

0.0540

closest p · 1.1× alpha

0.0540

boldest claim

The sentences

only marginally significantp = 0.054so close (0.05 < p ≤ 0.1)

In contrast, though only marginally significant, AFR PLWH with HP2 had lower risk ( OR = 0.111, p = 0.054) of developing NCI compared to people without HP2 ( Figure 2A ).

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