Barely Significant
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Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism.

Mol Autism · 2013 · PMC3903107 · PMID 24321478

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nominally significantno p-value reported
Additionally, a few haplotypes, including a 19 kb genomic region that formed a linkage disequilibrium (LD) block in our sample and contained several nominally significant SNPs, were found to be significantly associated with AS.

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