Barely Significant
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Identifying genes associated with obstructive congenital heart defects using a family-based genetic random field method.

HGG Adv · 2026 · PMC13445198 · PMID 42410936

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highly significantno p-value reported
When common and rare variants were analyzed jointly, the association became even more pronounced, yielding highly significant results in both phase I analysis and the combined analysis.

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