Barely Significant
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A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.

Nature · 2011 · PMC3266855 · PMID 22080950

1
hedged sentence
0.0003
closest p · 0.0× alpha
0.0003
boldest claim

The sentences

highly significantP = 0.0003actually significant
The association with melanoma in the pooled UK and Australian data was highly significant (combined P = 0.0003, OR 2.19, 95% CI 1.41–3.45).

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