Barely Significant
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Gene4MND: An Integrative Genetic Database and Analytic Platform for Motor Neuron Disease.

Front Mol Neurosci · 2021 · PMC8047132 · PMID 33867934

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highly significantno p-value reported
Multiple highly significant risk variants have also been successfully identified in genome-wide association studies (GWAS) (Nicolas et al., 2018 ; Farhan et al., 2019 ).

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