Barely Significant
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Do rare variant genotypes predict common variant genotypes?

BMC Proc · 2011 · PMC3287928 · PMID 22373504

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nominally significantP < 0.05actually significant
For each gene, the genotype score for a randomly chosen common SNP (common variant genotype score, CVGS) was regressed on the unweighted sums of genotype scores for all rare SNPs in the gene (sum of rare variant genotype scores, SRVGS), and the frequency of nominally significant ( P < 0.05) regressions was recorded.

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