Barely Significant
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Accurate and robust genomic prediction of celiac disease using statistical learning.

PLoS Genet · 2014 · PMC3923679 · PMID 24550740

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likely to be significantno p-value reported
The medical and economic impact of improving CD diagnosis is likely to be significant, and our findings support further studies into the role of personalized GRS's for other strongly heritable human diseases.

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