|(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 17684544] Systematic association mapping identifies NELL1 as a novel IBD disease gene.
[PMID 18070336] CD209 in inflammatory bowel disease: a case-control study in the Spanish population.
[PMID 18382655] Maternal TLR4 and NOD2 gene variants, pro-inflammatory phenotype and susceptibility to early-onset preeclampsia and HELLP syndrome.
[PMID 18650832] MAST3: a novel IBD risk factor that modulates TLR4 signaling.
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[PMID 19147066] Genomic and proteomic analysis of allogeneic hematopoietic cell transplant outcome. Seeking greater understanding the pathogenesis of GVHD and mortality.
[PMID 19185283] Searching for genotype-phenotype structure: using hierarchical log-linear models in Crohn disease.
[PMID 19557189] Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.
[PMID 19570052] NOD2/CARD15 genotype and common gastrointestinal diseases in 43,600 individuals.
[PMID 19843337] Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer.
[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.
[PMID 20371648] Penetrance of NOD2/CARD15 genetic variants in the general population.
[PMID 20646321] Toll-like receptor (TLR) and nucleosome-binding oligomerization domain (NOD) gene polymorphisms and endometrial cancer risk.
[PMID 21304977] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.
[PMID 21730793] Influence of Crohn's disease risk alleles and smoking on disease location.
[PMID 21745515] Role of NOD1/CARD4 and NOD2/CARD15 gene polymorphisms in cancer etiology.
[PMID 21830272] Distinct and overlapping genetic loci in Crohn's disease and ulcerative colitis: correlations with pathogenesis.
[PMID 22563200] Association of NOD1 and NOD2 genes polymorphisms with Helicobacter pylori related gastric cancer in a Chinese population.
[PMID 21745302] NOD2 gene variants are a risk factor for culture-positive spontaneous bacterial peritonitis and monomicrobial bacterascites in cirrhosis.
[PMID 23651603] P268S in NOD2 associates with susceptibility to Parkinson's disease in Chinese population
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