rs5743272, NOD2

N. diseases: 1
Disease: Crohn Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.710 GeneticVariation BEFREE Interestingly, we also found a rare variant in NOD2 previously associated with Crohn's disease (p.His352Arg). 30063981 2018
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.710 GeneticVariation UNIPROT Characterization and Genetic Analyses of New Genes Coding for NOD2 Interacting Proteins. 27812135 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.710 GeneticVariation UNIPROT Interaction between NOD2 and CARD9 involves the NOD2 NACHT and the linker region between the NOD2 CARDs and NACHT domain. 24960071 2014
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.710 GeneticVariation UNIPROT The molecular chaperone HSP70 binds to and stabilizes NOD2, an important protein involved in Crohn disease. 24790089 2014
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.710 GeneticVariation UNIPROT Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel disease. 16485124 2006
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.710 GeneticVariation UNIPROT Crohn disease: frequency and nature of CARD15 mutations in Ashkenazi and Sephardi/Oriental Jewish families. 15024686 2004
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.710 GeneticVariation UNIPROT Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. 11385576 2001