Due to the constitutive expression of this variant library, we predict that this population is likely representative of silent variants that exhibit WT-like p53 activity and are therefore dropped out of the population
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Further studies are needed to elucidate the predisposition of some variants toward certain clinical manifestations, particularly neonatal hyperbilirubinemia, and how some variants increase in severity when co-inherited with other blood- or bilirubin-related genetic disorders
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Its supporting evidence is animal and cell-culture research, which is genuinely interesting for understanding mechanism but doesn't establish human safety or efficacy at any particular dose