Barely Significant
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Exploring Health Care Disparities in Genetic Testing and Research for Hereditary Cardiomyopathy: Current State and Future Perspectives.

Glob Med Genet · 2024 · PMC10834107 · PMID 38304308

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possibly significantno p-value reported
We recommend expanding large-scale genetic studies such as next-generation sequencing in the research context so a more complete picture of both benign and possibly significant variants can be established.

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