A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation.

Commun Biol · 2024 · PMC10998918 · PMID 38582945

Europe PMC DOI

hedged sentence

0.0000

closest p · 0.0× alpha

0.0000

boldest claim

The sentences

nominally significantP = 2.61 × 10 −5actually significant

14 , a SNP at the PIDD1 gene locus reached suggestive significance 14 ( P = 7 × 10 −7 ), and our lead novel variants at SSBP3 and THSD7A were at least nominally significant ( P = 2.61 × 10 −5 and P = 0.025, respectively).

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