Barely Significant
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Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.

J Med Genet · 2018 · PMC6252362 · PMID 30166351

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hedged sentence
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closest p · 0.0× alpha
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boldest claim

The sentences

highly significantp=2.2×10 −130actually significant
Five genes associated with pigmentary traits were identified in the analysis with highly significant SNP associations: SLC45A2 (rs16891982, β=−0.546, SE=0.021, p=2.2×10 −130 ), IRF4 (rs12203592, β=1.915, SE=0.118, p=2.8×10 −57 ), HERC2 (rs1667394, β=−0.608, SE=0.02, p=2.8×10 −176 ), OCA2 (rs11855019, β=−0.548, SE=0.022, p=2.4×10 −121 ) and MC1R (rs1805007, β=3.615, SE=0.326, p=7.7×10 −22 ) (online supplementary figure S3 ).

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