Barely Significant
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Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.

Gut · 2013 · PMC3686259 · PMID 22543157

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The χ 2 analysis to test for an excess of deleterious rare variants in known and candidate IBD genes in IBD cases listed in table 2 compared to 22 reference exomes did not reach statistical significance (supplementary table 5).

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