|(C;C)||4||~35x higher risk for Crohn's disease|
|(C;G)||3||3x higher risk for Crohn's disease|
|(G;G)||0||common in complete genomics|
[PMID 18756601] No association was found for NOD2/CARD15 SNPs (R702W, G908R) in Chinese patients with inflammatory bowel disease.[PMID 19435634] Three-cohort targeted gene screening reveals a non-synonymous TRKA polymorphism associated with schizophrenia
[PMID 20412372] NOD2/CARD15 genotype, cardiovascular disease and cancer in 43,600 individuals from the general population
[PMID 20940596] NOD2/CARD15 Mutations Correlate With Severe Pouchitis After Ileal Pouch-Anal Anastomosis
[PMID 20959815] NOD2 Gene Polymorphism rs2066844 Associates With Need for Combined Liver-Intestine Transplantation in Children With Short-Gut Syndrome
[PMID 21206965] IL23R, NOD2/CARD15, ATG16L1 and PHOX2B polymorphisms in a group of patients with Crohn's disease and correlation with sub-phenotypes
[PMID 21734346] High-resolution melting curve analysis for high-throughput genotyping of NOD2/CARD15 mutations and distribution of these mutations in Slovenian inflammatory bowel diseases patients
[PMID 22269043] Clinical predictors of inflammatory bowel disease in a genetically well-defined Caucasian population
|Disease||INFLAMMATORY BOWEL DISEASE 1 (CROHN DISEASE) not specified Blau syndrome Crohn disease YAO SYNDROME|
|CLNDBN||INFLAMMATORY BOWEL DISEASE 1 (CROHN DISEASE), SUSCEPTIBILITY TO not specified Blau syndrome Crohn disease YAO SYNDROME, SUSCEPTIBILITY TO|
|CLNSRC||OMIM Allelic Variant UniProtKB (protein)|
|CLNACC||RCV000004956.4, RCV000238745.1, RCV000268347.1, RCV000363061.1, RCV000416490.1,|
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[PMID 20066736] Interaction of the major inflammatory bowel disease susceptibility alleles in Crohn's disease patients.
[PMID 20082483] NOD2, IL23R and ATG16L1 polymorphisms in Lithuanian patients with inflammatory bowel disease.
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[PMID 20646321] Toll-like receptor (TLR) and nucleosome-binding oligomerization domain (NOD) gene polymorphisms and endometrial cancer risk.
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