Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.

Mol Genet Genomic Med · 2018 · PMC6160704 · PMID 30008175

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nominally significantno p-value reported

However, we report on two nominally significant SNP s in two genes that have been implicated in the cognitive and social phenotypes of Williams syndrome, BAZ 1B and GTF 2 IRD 1 .

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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.