Barely Significant
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The hazards of genotype imputation when mapping disease susceptibility variants.

Genome Biol · 2024 · PMC10763476 · PMID 38172955

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highly significantno p-value reported
The 2014 meta-analysis identified only three of the eight significant TCF7L2 SNPs we studied here, and only the 2022 meta-analyses (which uses ~ 1.5-M cases/controls) identify all eight as highly significant (Table 3 ).

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