Barely Significant
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Evaluation of 22 genetic variants with Crohn's disease risk in the Ashkenazi Jewish population: a case-control study.

BMC Med Genet · 2011 · PMC3212904 · PMID 21548950

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A trend toward a higher frequency of the ATG16L1 rs2241880 and rs10210302 polymorphisms (in LD, D' = 0.99, r 2 = 0.96) was observed in CD cases compared to controls, but this association did not reach statistical significance.

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