Barely Significant
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Analysis of common and rare <i>VPS13C</i> variants in late-onset Parkinson disease.

Neurol Genet · 2020 · PMC6984134 · PMID 32042909

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In the 2 other cohorts, these variants showed the same directionality as in the New York cohort but did not reach statistical significance ( table 2 ).

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nominally significantno p-value reported
These remained nominally significant with and without including adjustment for ethnicity, suggesting that ethnicity has no role in this association and only one of them, p.

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