Barely Significant
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Machine Learning SNP Based Prediction for Precision Medicine.

Front Genet · 2019 · PMC6445847 · PMID 30972108

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highly significantno p-value reported
Early attempts to use weighted polygenic risk scores, were based on small numbers of highly significant SNPs identified from GWA studies, and achieved only limited predictive value for complex diseases ( Amin et al., 2009 ; Dudbridge, 2013 ).

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