Transcription factor 7-like 2 (TCF7L2) variant is associated with familial breast cancer risk: a case-control study.

BMC Cancer · 2006 · PMC1665524 · PMID 17109766

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closest p · 0.8× alpha

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boldest claim

The sentences

borderline significanceP = 0.04actually significant

Results The T allele of rs12255372 showed an association with borderline significance (OR = 1.19, 95% C.I. = 1.01-1.42, P = 0.04), and the Cochran-Armitage test for trend revealed an allele dose-dependent association of rs12255372 with BC risk ( P trend = 0.04).

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