Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures.

Elife · 2016 · PMC4862755 · PMID 27162171

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nominally significantno p-value reported

p=1x10 -4 to 5x10 -8 , Figure 3b ), likely due to removal of nominally significant SNPs that are in LD with above-threshold QT/QRS loci and do not represent true association signals.

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