Barely Significant
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Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis.

Hum Mol Genet · 2013 · PMC3554206 · PMID 23193196

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highly significantno p-value reported
The P -values for tests of the estimates being different from zero for all three diseases were highly significant (Table 1 ).

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