Barely Significant
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A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.

Hum Genet · 2012 · PMC3303079 · PMID 21996756

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highly significantp = 0.001actually significant
While the odds ratio decreased slightly, it remained highly significant, indicating that there is an association between rHH status and ASD status that is independent of gene size [size adjusted p = 0.001, OR = 2.10, (1.36, 3.25)].

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