Barely Significant
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Exome sequencing in genetic disease: recent advances and considerations.

F1000Res · 2020 · PMC7205110 · PMID 32431803

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may be significantno p-value reported
If a variant alters the coding sequence of a protein (that is, if the variant is non-synonymous or induces a premature termination of the protein), the effect on the translated protein may be significant.

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