Barely Significant
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Genotype-based test in mapping cis-regulatory variants from allele-specific expression data.

PLoS One · 2012 · PMC3369843 · PMID 22685595

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highly significantp = 2.5×10 −7actually significant
Note, however, that in the same time, both haplotype based tests reveal a number of significant SNPs (one highly significant, p = 2.5×10 −7 , in the case of linear regression) among those within the transcript itself and used as informative markers for the detection of AI.

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