Barely Significant
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Analysis of damaging non-synonymous SNPs in GPx1 gene associated with the progression of diverse cancers through a comprehensive in silico approach.

Sci Rep · 2024 · PMC11577101 · PMID 39562776

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highly significantno p-value reported
Based on the already submitted information, ClinVar categorized all of the three mutants (G75C, F167S, L168Q) as highly significant for clinical profiles.

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