Barely Significant
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Whole genome sequencing in support of wellness and health maintenance.

Genome Med · 2013 · PMC3967117 · PMID 23806097

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highly significantno p-value reported
Note that these analyses only include highly significant genotypes from GWAS that have been independently replicated, thus they capture a minor proportion of the suspected genetic variance, and consequently there is not a strong expectation at this stage of genomic medicine that the relatively small genotypic samples should be predictive [ 31 , 32 ].

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