Barely Significant
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Fine-mapping of Parkinson's disease susceptibility loci identifies putative causal variants.

Hum Mol Genet · 2022 · PMC8947317 · PMID 34617105

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highly significantno p-value reported
This association remained highly significant even after background correction and stringent Bonferroni multiple-testing correction ( q < 1x10 −10 ).

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