Barely Significant
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Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C).

J Exp Med · 2024 · PMC11586762 · PMID 39576310

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nominally significantno p-value reported
Notably, two of the largest ancestral groups in our MIS-C cohort (EUR and AMR) exhibit a standalone statistically significant burden, while the other two (AFR and SAS) are nominally significant.

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