Barely Significant
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Delving Into the Depths of <i>AGTR2</i>: In Silico Identification of Deleterious Nonsynonymous SNPs Associated With Cardiovascular Diseases.

Hum Mutat · 2026 · PMC13084195 · PMID 42006151

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highly significantno p-value reported
Moreover, ClinVar database further evaluated all of the four shortlisted mutants as highly significant for clinical profiles, based on the already submitted information. 3.7.

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