Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1.

Genet Mol Biol · 2018 · PMC5901500 · PMID 29473935

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nominally significantno p-value reported

Corroborating, a nominally significant single-marker association of SNP rs600753 with spelling was identified in German dyslexia families ( Matsson et al. , 2015 ).

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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.