Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519328
rs1057519328
C 0.700 CausalMutation CLINVAR

dbSNP: rs146597836
rs146597836
T 0.700 CausalMutation CLINVAR

dbSNP: rs746055479
rs746055479
T 0.700 CausalMutation CLINVAR

dbSNP: rs750868279
rs750868279
A 0.700 CausalMutation CLINVAR

dbSNP: rs751454741
rs751454741
T 0.700 CausalMutation CLINVAR

dbSNP: rs752615209
rs752615209
T 0.700 CausalMutation CLINVAR

dbSNP: rs755659290
rs755659290
C 0.700 CausalMutation CLINVAR

dbSNP: rs774164456
rs774164456
C 0.700 CausalMutation CLINVAR

dbSNP: rs886039866
rs886039866
A 0.700 CausalMutation CLINVAR

dbSNP: rs886040969
rs886040969
A 0.700 CausalMutation CLINVAR

dbSNP: rs751377893
rs751377893
F5
0.030 GeneticVariation BEFREE We investigated the prevalence of the coagulation factor V gene G1691A mutation in 64 patients with Behçet's disease (BD) and in 107 apparently healthy individuals. 8948311

1996

dbSNP: rs1217691063
rs1217691063
0.090 GeneticVariation BEFREE MTHFR gene C677T mutation does not increase risk of DVT in BD either alone or combined with FV Leiden mutation. 11128675

2000

dbSNP: rs3743930
rs3743930
0.050 GeneticVariation BEFREE The M694V, V726A and E148Q mutations tended to be more frequent in definite BD (2.6%, 2.6%, and 5.2%, respectively) than in controls (0%, 0%, and 2.2%). 10980540

2000

dbSNP: rs61752717
rs61752717
0.040 GeneticVariation BEFREE The M694V, V726A and E148Q mutations tended to be more frequent in definite BD (2.6%, 2.6%, and 5.2%, respectively) than in controls (0%, 0%, and 2.2%). 10980540

2000

dbSNP: rs1188383936
rs1188383936
F2
0.030 GeneticVariation BEFREE MTHFR gene C677T mutation does not increase risk of DVT in BD either alone or combined with FV Leiden mutation. 11128675

2000

dbSNP: rs899127658
rs899127658
F2
0.030 GeneticVariation BEFREE Possible roles of methylenetetrahydrofolate reductase (MTHFR) gene C677T, factor V (FV) gene G1691A (Leiden), and prothrombin gene G20210A polymorphisms in venous thrombogenesis were evaluated in patients with BD; 100 healthy people, 30 BD patients without DVT, 30 BD patients with DVT, and 30 patients with idiopathic DVT were studied with the restriction fragment length polymorphism method for these 3 polymorphisms. 11128675

2000

dbSNP: rs28940579
rs28940579
0.020 GeneticVariation BEFREE The M694V, V726A and E148Q mutations tended to be more frequent in definite BD (2.6%, 2.6%, and 5.2%, respectively) than in controls (0%, 0%, and 2.2%). 10980540

2000

dbSNP: rs1799969
rs1799969
0.030 GeneticVariation BEFREE Our findings show that G/R 241 polymorphism of ICAM-1 is associated with BD susceptibility. 11409120

2001

dbSNP: rs1217691063
rs1217691063
0.090 GeneticVariation BEFREE The rates of homozygosity for the MTHFR C677T mutation in the BD and HC groups were 7.5% and 10%, respectively. 14504916

2003

dbSNP: rs1799983
rs1799983
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

dbSNP: rs1061622
rs1061622
0.010 GeneticVariation BEFREE In this study, we investigated genetic polymorphisms of TNF alpha -308 G/A, TNF beta +252 G/A, and TNFR2 196 R/M in 94 Korean BD patients and age- and sex-matched healthy controls to investigate the role of TNF and TNF receptor polymorphisms in BD. 12770792

2003

dbSNP: rs751377893
rs751377893
F5
0.030 GeneticVariation BEFREE To evaluate the frequency and type of vascular lesions and to study the association of factor V gene G1691A (Leiden) and prothrombin gene G20210A polymorphisms with venous thrombosis in Italian patients with Behçet's disease (BD). 15077257

2004

dbSNP: rs899127658
rs899127658
F2
0.030 GeneticVariation BEFREE To evaluate the frequency and type of vascular lesions and to study the association of factor V gene G1691A (Leiden) and prothrombin gene G20210A polymorphisms with venous thrombosis in Italian patients with Behçet's disease (BD). 15077257

2004

dbSNP: rs28940579
rs28940579
0.020 GeneticVariation BEFREE The frequencies of three FMF-related MEFV mutations (M694V, M680I and V726A) were investigated in BD patients (n = 57) by molecular genetic studies using a polymerase chain reaction with the ARMS method. 14727457

2004

dbSNP: rs2010963
rs2010963
0.010 GeneticVariation BEFREE All patients with BD and controls were genotyped by polymerase chain reaction and allele-specific oligonucleotide techniques for +936 C/T (rs3025039) and -634 C/G (rs2010963) mutations and for an 18 base pair (bp) insertion/deletion (I/D) polymorphism at -2549 of the the VEGF promoter region. 15338501

2004