Disease: Crohn Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104895423
rs104895423
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation UNIPROT Characterization and Genetic Analyses of New Genes Coding for NOD2 Interacting Proteins. 27812135 2016
dbSNP: rs104895423
rs104895423
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation UNIPROT The molecular chaperone HSP70 binds to and stabilizes NOD2, an important protein involved in Crohn disease. 24790089 2014
dbSNP: rs104895423
rs104895423
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		0.700 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: rs104895423
rs104895423
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		0.700 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: rs104895423
rs104895423
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation UNIPROT Crohn disease: frequency and nature of CARD15 mutations in Ashkenazi and Sephardi/Oriental Jewish families. 15024686 2004
dbSNP: rs104895423
rs104895423
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease:
Crohn Disease 		0.700 GeneticVariation UNIPROT Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. 11385576 2001