Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2066845
rs2066845
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0020875
Disease:
Ileal Diseases
0.010 GeneticVariation BEFREE The R702W, G908R, and 3020insC mutations are strong independent risk factors for CD and are associated particularly with ileal disease. 11910337 2002