A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures.

Hum Mol Genet · 2021 · PMC8188402 · PMID 33864365

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only marginally significantno p-value reported

Other studies combined analyses for language and reading abilities using both a case–control ( 36 ) and quantitative design ( 37 ) reporting only marginally significant associations.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.