Disease: Behcet Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs758548184
rs758548184
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0004943
Disease:
Behcet Syndrome 		0.010 GeneticVariation BEFREE We analysed the SNPs -318C/T and 49A/G in CTLA-4 in patients with Behcet's disease (BD), patients with intermediate uveitis and appropriate controls. 18498289 2008