Barely Significant
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Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci.

PLoS Genet · 2019 · PMC6407791 · PMID 30807572

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may be significantno p-value reported
Evaluation through simulation: Type 1 error of SS and false positive rate of COLOC and eCAVIAR For type 1 error evaluation, we considered a comprehensive set of null cases where Case 1 represents the simple null of no association and no eQTL, while Cases 2–4 correspond to composite null scenarios where for example both association and eQTL may be significant but distinct.

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