Barely Significant
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Confirmation of GRHL2 as the gene for the DFNA28 locus.

Am J Med Genet A · 2013 · PMC3884766 · PMID 23813623

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marginal significanceno p-value reported
In addition, several single nucleotide polymorphisms (SNPs) in GRHL2 have been associated with marginal significance with age-related hearing impairment susceptibility [Van Laer et al., 2008 ].

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marginally significantno p-value reported
In this light, it may also be worth following up the marginally significant association of presbycusis with GRHL2 variants [Van Laer et al., 2008 ], using larger cohorts.

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