Barely Significant
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Shared and unique common genetic determinants between pediatric and adult celiac disease.

BMC Med Genomics · 2016 · PMC4957920 · PMID 27449795

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highly significantno p-value reported
Cis-eQTL evaluation of the suggestive risk variants that we observed in the study, indicated highly significant functional relevance of 11 (35.5 %) risk variants which were seen to alter the level of gene expression at these loci (Additional file 2 : Table S3).

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