Disease: Behcet Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs752615209
rs752615209
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0004943
Disease:
Behcet Syndrome 		T 0.700 CausalMutation CLINVAR