Barely Significant
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Human inversions and their functional consequences.

Brief Funct Genomics · 2015 · PMC4576756 · PMID 25998059

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highly significantno p-value reported
This is exemplified by LRRC37A , whose expression shows highly significant differences between the 17q21.31 inversion alleles in several brain tissues, but the probes used are able to bind more than one target gene in the family [ 105 ].

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