Barely Significant
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Clinical Variant Reclassification in Hereditary Disease Genetic Testing.

JAMA Netw Open · 2024 · PMC11541632 · PMID 39504018

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a clear trendno p-value reported
Overall, we observed a clear trend where VUS with more pathogenic evidence were more likely to be reclassified as LP or pathogenic, while VUS with more benign evidence were more likely to be reclassified as LB or benign.

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