Barely Significant
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Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era.

Appl Clin Genet · 2012 · PMC3492098 · PMID 23144566

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highly significantno p-value reported
18 , 120 – 122 Despite a few highly significant findings that have led, for example, to identification of functional SNPs in candidate genes, 123 one of the most important collective contributions of these studies has been the confirmation that there is no unifying single gene mutation for familial forms of schizophrenia.

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