Barely Significant
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Allele-Specific Regulation of the Candidate Autism Liability Gene <i>RAI1</i> by the Enhancer Variant rs4925102 (<i>C/G</i>).

Genes (Basel) · 2024 · PMC11049881 · PMID 38674394

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nominally significantno p-value reported
As shown in Table 1 , these studies yield a nominally significant correlation of G/C odds ratios in the case-control study and a near-significance correlation in the TCT study, with the “low-expression” G -allele identified as the risk allele in both studies.

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