Barely Significant
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Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population.

BMC Genomics · 2017 · PMC5549306 · PMID 28789618

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marginal significanceno p-value reported
Conclusions We identified deletions in SFMBT1 that were significantly associated with FPG in the SAPPHIRe sample, and the deletions also showed marginal significance in the TWB sample.

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