Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4986790
rs4986790
0.020 GeneticVariation BEFREE No linkage or association was seen for Asp299Gly or Thr399Ile SNPs of TLR4 with JIA susceptibility. 15498795

2005

dbSNP: rs4986791
rs4986791
0.020 GeneticVariation BEFREE No linkage or association was seen for Asp299Gly or Thr399Ile SNPs of TLR4 with JIA susceptibility. 15498795

2005

dbSNP: rs2476601
rs2476601
0.090 GeneticVariation BEFREE Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases. 15759012

2005

dbSNP: rs1217691063
rs1217691063
0.030 GeneticVariation BEFREE To study the relationship of C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene to toxicity and efficacy of methotrexate (MTX) in patients with juvenile idiopathic arthritis (JIA). 16142884

2005

dbSNP: rs397507444
rs397507444
0.020 GeneticVariation BEFREE To study the relationship of C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene to toxicity and efficacy of methotrexate (MTX) in patients with juvenile idiopathic arthritis (JIA). 16142884

2005

dbSNP: rs237025
rs237025
0.010 GeneticVariation BEFREE The M55V substitution in the SUMO4 gene is not associated with susceptibility to RA or JIA in the UK population studied. 16159953

2005

dbSNP: rs2476601
rs2476601
0.090 GeneticVariation BEFREE The minor allele of the R620W missense single-nucleotide polymorphism (SNP; rs2476601) in the PTPN22 (protein tyrosine phosphatase non-receptor 22) gene has been reported to be associated with multiple autoimmune diseases, including type 1 diabetes, systemic lupus erythematosus, rheumatoid arthritis, juvenile idiopathic arthritis, autoimmune thyroiditis and vitiligo. 16464986

2006

dbSNP: rs2476601
rs2476601
0.090 GeneticVariation BEFREE This meta-analysis showed the association between the T-allele and the T/T genotype and JIA (OR = 1.34, P = 0.03; OR = 1.97, P = 0.02) but did not reveal the association between the PTPN22 C1858T polymorphism and IBD, psoriasis, multiple sclerosis, Addison's disease and Celiac disease. 16760194

2007

dbSNP: rs2476601
rs2476601
0.090 GeneticVariation BEFREE Its +1858C>T (R620W) polymorphism has been shown to associate with a risk for multiple autoimmune diseases, including type 1 diabetes (T1D) and juvenile idiopathic arthritis (JIA). 17000021

2007

dbSNP: rs231775
rs231775
0.010 GeneticVariation BEFREE These results suggest that C-318T, A49G, CT60, and haplotypes tagged by these CTLA4 SNPs are not associated with JIA or major JIA subtypes. 18576317

2008

dbSNP: rs2395148
rs2395148
0.800 GeneticVariation GWASCAT Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis. 18576341

2008

dbSNP: rs2395148
rs2395148
0.800 GeneticVariation GWASDB Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis. 18576341

2008

dbSNP: rs2104286
rs2104286
0.010 GeneticVariation BEFREE SNP rs2104286 within the IL2RA/CD25 gene was significantly associated with UK JI</span>A cases (OR for the allele 0.76 [95% CI 0.66-0.88], P for trend=0.0002). 19116909

2009

dbSNP: rs41295061
rs41295061
0.010 GeneticVariation BEFREE A second SNP (rs41295061) also showed modest evidence for association with JIA (OR 0.80 [95% CI 0.63-1.0], P=0.05). 19116909

2009

dbSNP: rs12046117
rs12046117
0.800 GeneticVariation GWASDB Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis. 19116933

2009

dbSNP: rs12046117
rs12046117
0.800 GeneticVariation GWASCAT Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis. 19116933

2009

dbSNP: rs1042713
rs1042713
0.010 GeneticVariation BEFREE Genotypes and haplotypes of two ADRB2 variants (G16R and Q27E) were determined in 348 children with JIA and 448 healthy controls by direct molecular haplotyping using melting-curve analysis of a fluorescently labelled loci-spanning probe. 19177262

2009

dbSNP: rs1042714
rs1042714
0.010 GeneticVariation BEFREE Genotypes and haplotypes of two ADRB2 variants (G16R and Q27E) were determined in 348 children with JIA and 448 healthy controls by direct molecular haplotyping using melting-curve analysis of a fluorescently labelled loci-spanning probe. 19177262

2009

dbSNP: rs2476601
rs2476601
0.090 GeneticVariation BEFREE However, C1858T polymorphism of PTPN22, another candidate gene of autoimmunity seems to be independent of JIA in Hungarian patients. 19210888

2009

dbSNP: rs10499194
rs10499194
0.010 GeneticVariation BEFREE The strongest associations with JIA risk or protection were observed for TNFAIP3 variants rs10499194 (OR 0.74 [95% CI 0.61-0.91], P < 0.004) and rs6920220 (OR 1.30 [95% CI 1.05-1.61], P = 0.015). 19565500

2009

dbSNP: rs6920220
rs6920220
0.010 GeneticVariation BEFREE The strongest associations with JIA risk or protection were observed for TNFAIP3 variants rs10499194 (OR 0.74 [95% CI 0.61-0.91], P < 0.004) and rs6920220 (OR 1.30 [95% CI 1.05-1.61], P = 0.015). 19565500

2009

dbSNP: rs12708716
rs12708716
0.010 GeneticVariation BEFREE The intron 22 SNP, rs6498169, was associated with RA (p=0.006) and JIA (p=0.016) and the intron 19 SNPs, rs12708716/rs12917716, with T1D (p=1x10-5) and AD (p=2x10-4). 19734133

2010

dbSNP: rs12917716
rs12917716
0.010 GeneticVariation BEFREE The intron 22 SNP, rs6498169, was associated with RA (p=0.006) and JIA (p=0.016) and the intron 19 SNPs, rs12708716/rs12917716, with T1D (p=1x10-5) and AD (p=2x10-4). 19734133

2010

dbSNP: rs6498169
rs6498169
0.010 GeneticVariation BEFREE The intron 22 SNP, rs6498169, was associated with RA (p=0.006) and JIA (p=0.016) and the intron 19 SNPs, rs12708716/rs12917716, with T1D (p=1x10-5) and AD (p=2x10-4). 19734133

2010

dbSNP: rs1217691063
rs1217691063
0.030 GeneticVariation BEFREE To investigate whether methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms and erythrocyte concentration of methotrexate (EMTX) could serve as predictors of methotrexate (MTX) efficacy and toxicity in patients with juvenile idiopathic arthritis (JIA). 20595278

2010