Barely Significant
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A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human.

Nucleic Acids Res · 2018 · PMC5909433 · PMID 29518216

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hedged sentence
0.0000
closest p · 0.0× alpha
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boldest claim

The sentences

highly significantP < 5 × 10 −8actually significant
Importantly, while the P -value for rs17421627 and rs1568679 are highly significant with the common standards used in GWAS ( P < 5 × 10 −8 ), this is not the case for rs16932455 ( P = 2 × 10 −6 ).

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