A method for scoring the cell type-specific impacts of noncoding variants in personal genomes.

Proc Natl Acad Sci U S A · 2020 · PMC7474608 · PMID 32817564

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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 = 3.4 × 10 −32actually significant

This is a 200-kb region centering at a highly significant risk SNP rs12579077 ( P = 3.4 × 10 −32 ) 2 kb upstream of IGF1.

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