Barely Significant
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Uncovering genetic associations in the human diseasome using an endophenotype-augmented disease network.

Bioinformatics · 2024 · PMC10963079 · PMID 38527901

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highly significantno p-value reported
116 indirect edges represented the same cross-phenotype associations as pre-existing direct edges, suggesting that highly significant SNPs associated with disease associations may be involved in the same pathways as the biomarkers that connect them.

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