Barely Significant
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Identification of common genetic variation that modulates alternative splicing.

PLoS Genet · 2007 · PMC1904363 · PMID 17571926

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highly significantno p-value reported
We identified 70 simple cassette exon alternative splicing events in our experimental system; for six of these, we detected consistent differences in splicing pattern between individuals, with a highly significant association between splice phenotype and neighbouring SNPs.

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