Barely Significant
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An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients.

Genes (Basel) · 2021 · PMC8535321 · PMID 34681001

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nominally significantno p-value reported
More specifically, we filtered out variants whose association with MS susceptibility was not significant among any of these cohorts, whereas we only retained variants that were at least nominally significant or absent in any of the aforementioned large MS datasets.

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