Barely Significant
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Genetic modulation of oxytocin sensitivity: a pharmacogenetic approach.

Transl Psychiatry · 2015 · PMC4930136 · PMID 26506050

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nominally significantno p-value reported
As shown in Table 3 , the A-allele of rs2254298, which also shows a nominally significant association on the single SNP level, falls exclusively on the significant haplotype.

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