Genetic variants associated with Crohn's disease.

Appl Clin Genet · 2013 · PMC3735034 · PMID 23935379

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highly significantno p-value reported

Deep resequencing of GWAS data has identified highly significant variants at CARD9, NOD2/CARD15 , CUL2, and IL18RAP, which contribute to risk associations of previously defined variants at these loci, and as well, showed the functionality of the newly implicated NOD2/CARD15 variants.

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