Barely Significant
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Genetic variation in the oxytocin receptor (OXTR) gene is associated with Asperger Syndrome.

Mol Autism · 2014 · PMC4175274 · PMID 25264479

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nominally significantno p-value reported
have previously reported a nominally significant association between this SNP and a narrow ASC diagnosis in family-based samples [ 27 ].

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