Barely Significant
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Leveraging family history in genetic association analyses of binary traits.

BMC Genomics · 2022 · PMC9526325 · PMID 36182916

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near-significantno p-value reported
In general, adding family history information resulted in a more drastic change in association results from CC-GWAS to LT-FH, given the overall reduction in the number of significant and near-significant genetic variants detected by LT-FH.

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