Barely Significant
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Genetic underpinnings of the psoriatic spectrum.

Med Genet · 2023 · PMC10842586 · PMID 38835412

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highly significantno p-value reported
In a study examining CNVs associated with PsA, a highly significant association of an intergenic deletion of ~26 kb between ADAMTS9 and MAGI1 was detected.

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