Disease: Behcet Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs746055479
rs746055479
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0004943
Disease:
Behcet Syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs752615209
rs752615209
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0004943
Disease:
Behcet Syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs886040969
rs886040969
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0004943
Disease:
Behcet Syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs2066844
rs2066844
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0004943
Disease:
Behcet Syndrome 		0.020 GeneticVariation BEFREE Our results suggest that the association of MEFV with BD could be modulated by the HLA molecules; whereas the protective effect of NOD2 p.Arg702Trp would be independent of HLA. 30808881 2019
dbSNP: rs2066844
rs2066844
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0004943
Disease:
Behcet Syndrome 		0.020 GeneticVariation BEFREE Both the Arg702Trp and Leu1007fs (frameshift) variants were significantly less frequently present among BD patients compared with healthy controls (0.5 vs 5.8%; P < 1.10(-5) and 0.0 vs 1.8%; P < 0.007, respectively). 19748964 2009
dbSNP: rs2066845
rs2066845
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0004943
Disease:
Behcet Syndrome 		0.010 GeneticVariation BEFREE It has been shown previously that three nucleotide-binding oligomerization domain containing 2 (NOD2) variants (Arg702Trp, Gly908Arg and Lue1007fs) are associated with Crohn's disease (CD), a disorder clinically resembling Behçet's disease (BD). 19748964 2009
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