Barely Significant
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Whole-genome sequencing reveals novel ethnicity-specific rare variants associated with Alzheimer's disease.

Mol Psychiatry · 2022 · PMC9135624 · PMID 35264725

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nominally significantno p-value reported
From our variant-based association study, we first discovered an Asian-specific rare heterozygous missense variant in OR51G1 showing a nominally significant association with the same direction of effect in the both the discovery and replication sets.

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