Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799983
rs1799983
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.070 GeneticVariation BEFREE The result showed a decreased frequency of the NOS3/rs1799983 GG genotype and an increased frequency of NOS3/rs1799983 GT genotype in the patients with BD (Bonferroni correction test [Pc]=0.02, odds ratio [OR]=0.74; Pc=2.1×10(-3), OR=1.57, respectively). 27114698

2016

dbSNP: rs1799983
rs1799983
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.070 GeneticVariation BEFREE These results suggest that Glu298Asp polymorphism of the NOS3 gene is associated with BD susceptibility in Tunisian patients. 25639851

2015

dbSNP: rs1799983
rs1799983
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.070 GeneticVariation BEFREE This meta-analysis shows that the eNOS G894T and the 4b/a polymorphisms are not associated with BD in the Turkish and Asian populations. 21957880

2012

dbSNP: rs1799983
rs1799983
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.070 GeneticVariation BEFREE Our findings suggest that Glu298Asp polymorphism of eNOS gene is associated with BD susceptibility as well as skin lesions. 18718857

2008

dbSNP: rs1799983
rs1799983
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.070 GeneticVariation BEFREE In this study, we found that Glu298Asp polymorphism of the eNOS gene was associated with BD in Turkish patients. 17067432

2007

dbSNP: rs1799983
rs1799983
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.070 GeneticVariation BEFREE Glu298 --> Asp polymorphism of the eNOS gene does not appear to be associated with the presence of BD in the Turkish population. 16463158

2006

dbSNP: rs1799983
rs1799983
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.070 GeneticVariation BEFREE The Glu298Asp polymorphism in exon 7 of the eNOS gene seems to be a susceptibility gene for Korean BD and other rheumatic diseases. 14583572

2003