Does the inclusion of rare variants improve risk prediction?

BMC Proc · 2014 · PMC4143761 · PMID 25519349

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marginal significanceno p-value reported

Implementation We restricted our study to the top 1000 CV SNPs and top 1000 RV SNPs as identified by the marginal significance of a Kruskal-Wallis test of the minor allele counts and SBP values for the 759 samples.

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