Barely Significant
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SNPs selection using support vector regression and genetic algorithms in GWAS.

BMC Genomics · 2014 · PMC4243330 · PMID 25573332

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highly significantno p-value reported
So far, the prediction of disease risk in humans based on validated SNPs based on this methodology showed little predictive power [ 2 ], although these SNPs indicate highly significant association with the phenotypic trait.

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