Barely Significant
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Identification and Evolutionary Analysis of Potential Candidate Genes in a Human Eating Disorder.

Biomed Res Int · 2016 · PMC4819096 · PMID 27088090

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only marginally significantno p-value reported
This is particularly notable in VGF, which appears to have a preponderance of mutations predicted to be poorly tolerated relative to other genes examined in this study (though this excess of poorly tolerated variation is only marginally significant compared to other proteins examined).

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