Barely Significant
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Examination of candidate exonic variants for association to Alzheimer disease in the Amish.

PLoS One · 2015 · PMC4323242 · PMID 25668194

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closest p
boldest claim

The sentences

nominally significantno p-value reported
The criteria for prioritization were a nominally significant association p-value (< 0.01) in the sequencing data or because the variant was not present in three catalogs of human variation (dbSNP build 137, ESP 6500 release, and 1000 Genomes April 2012 release).

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