Barely Significant
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Large-scale risk prediction applied to Genetic Analysis Workshop 17 mini-exome sequence data.

BMC Proc · 2011 · PMC3287883 · PMID 22373389

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highly significantno p-value reported
Under the simulation design for the GAW17 data set, if a large proportion of rare variants are involved in this data set, then we need to record the number of SNPs and the minor allele frequency (MAF) interval of SNPs within these highly significant genes (see Table 1 ).

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