Barely Significant
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Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans.

Commun Biol · 2022 · PMC9061855 · PMID 35501403

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highly significantno p-value reported
These inter-ethnic discrepancies in the MAFs and the differences between disparate biological samples (serum copper and erythrocytes copper) may explain the highly significant association of rs2769264 in Europeans and no significant association in East Asians 36 .

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