Individual common variants exert weak effects on the risk for autism spectrum disorders.

Hum Mol Genet · 2012 · PMC3471395 · PMID 22843504

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marginally significantno p-value reported

We performed four primary association analyses based on ancestry and clinical thresholds and identified a single, marginally significant association for SNP rs4141463 located within MACROD2 .

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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.