Barely Significant
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Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population.

Front Genet · 2021 · PMC8762330 · PMID 35047017

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nominally significantno p-value reported
We adopted an exploratory approach and nominated for follow up in the replication phase those genes detected as nominally significant in any of the seven scenarios according to the hybrid test.

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