Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5743272
rs5743272
NOD2
0.710 GeneticVariation BEFREE Interestingly, we also found a rare variant in NOD2 previously associated with Crohn's disease (p.His352Arg). 30063981

2018
dbSNP: rs5743272
rs5743272
NOD2
0.710 GeneticVariation UNIPROT Characterization and Genetic Analyses of New Genes Coding for NOD2 Interacting Proteins. 27812135

2016
dbSNP: rs5743272
rs5743272
NOD2
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
dbSNP: rs5743272
rs5743272
NOD2
0.710 GeneticVariation UNIPROT The molecular chaperone HSP70 binds to and stabilizes NOD2, an important protein involved in Crohn disease. 24790089

2014
dbSNP: rs5743272
rs5743272
NOD2
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
dbSNP: rs5743272
rs5743272
NOD2
0.710 GeneticVariation UNIPROT Crohn disease: frequency and nature of CARD15 mutations in Ashkenazi and Sephardi/Oriental Jewish families. 15024686

2004
dbSNP: rs5743272
rs5743272
NOD2
0.710 GeneticVariation UNIPROT Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. 11385576

2001