Barely Significant
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Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort.

Parkinsonism Relat Disord · 2022 · PMC10112543 · PMID 35917738

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nominally significantno p-value reported
In LARGE-PD, hap6 and hap11 were nominally significant (p-value 0.039 and 2.65 × 10 − 5 , respectively) while hap9 was not (p-value 0.076).

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