Barely Significant
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Family-based exome sequencing identifies rare coding variants in age-related macular degeneration.

Hum Mol Genet · 2020 · PMC7390936 · PMID 32246154

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showed a trendno p-value reported
While we did not observe a significant difference [at false discovery rate (FDR) ≤ 10%] during disease progression, several candidates showed a trend of either increased or decreased expression ( Fig. 3B ).

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