Barely Significant
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Identification of a 31-bp deletion in the RELN gene causing lissencephaly with cerebellar hypoplasia in sheep.

PLoS One · 2013 · PMC3834269 · PMID 24260534

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hedged sentence
closest p
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The sentences

highly significantno p-value reported
The SNP showing the most highly significant association was OAR4_45088426, which is located at position 42,810,217 bp in the OARv3.1 ovine genome sequence.

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