Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD.

BMC Med Genet · 2008 · PMC2322963 · PMID 18384690

Europe PMC DOI

hedged sentence

0.0400

closest p · 0.8× alpha

0.0400

boldest claim

The sentences

nominally significantP = 0.04actually significant

For LOX1.3, the minor allele showed a nominally significant association with clinical CHD but in the opposite direction than that seen in the ADVANCE study (HRR 0.92, P = 0.04 for the additive model).

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