Barely Significant
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An evolutionary framework for association testing in resequencing studies.

PLoS Genet · 2010 · PMC2978703 · PMID 21085648

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nominally significantno p-value reported
An interesting data point in Figure 3 is a single 5% frequency non-coding variant (directly before R278Q) whose OLS effect estimate is quite large (and nominally significant) but whose model-based effect estimate is small.

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