Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104895460
rs104895460
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0042164
Disease:
Uveitis
0.010 GeneticVariation BEFREE Three main mutations in this gene (R334W, R334Q and L469F) have been reported as Blau syndrome risk factors, a disease that manifests uveitis as one of its clinical features. 19822951 2009