Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11265618
rs11265618
0.010 GeneticVariation BEFREE In the present study, we aimed to investigate the influence of clinical parameters and single-nucleotide polymorphisms of interleukin-6 receptor (rs12083537, rs2228145, rs4329505 and rs11265618) on response to tocilizumab, TCZ (European League Against Rheumatism (EULAR) response, remission, low disease activity (LDA) and improvement of DAS28). 27958380

2018

dbSNP: rs11541076
rs11541076
0.010 GeneticVariation BEFREE Primary analyses validated the IRAK3 rs11541076 variant as associated (odds ratio (OR)=1.33, 95% confidence interval (CI): 1.00-1.77, P-value=0.047) with a positive treatment response (EULAR (European League Against Rheumatism) good/moderate vs none response at 4±2 months), and found the NLRP3 rs461266 variant associated (OR=0.75, 95% CI: 0.60-0.94, P=0.014) with a negative treatment response. 27698401

2018

dbSNP: rs2228145
rs2228145
0.010 GeneticVariation BEFREE In the present study, we aimed to investigate the influence of clinical parameters and single-nucleotide polymorphisms of interleukin-6 receptor (rs12083537, rs2228145, rs4329505 and rs11265618) on response to tocilizumab, TCZ (European League Against Rheumatism (EULAR) response, remission, low disease activity (LDA) and improvement of DAS28). 27958380

2018

dbSNP: rs4329505
rs4329505
0.010 GeneticVariation BEFREE In the present study, we aimed to investigate the influence of clinical parameters and single-nucleotide polymorphisms of interleukin-6 receptor (rs12083537, rs2228145, rs4329505 and rs11265618) on response to tocilizumab, TCZ (European League Against Rheumatism (EULAR) response, remission, low disease activity (LDA) and improvement of DAS28). 27958380

2018

dbSNP: rs461266
rs461266
0.010 GeneticVariation BEFREE Primary analyses validated the IRAK3 rs11541076 variant as associated (odds ratio (OR)=1.33, 95% confidence interval (CI): 1.00-1.77, P-value=0.047) with a positive treatment response (EULAR (European League Against Rheumatism) good/moderate vs none response at 4±2 months), and found the NLRP3 rs461266 variant associated (OR=0.75, 95% CI: 0.60-0.94, P=0.014) with a negative treatment response. 27698401

2018

dbSNP: rs2230926
rs2230926
0.010 GeneticVariation BEFREE TNFAIP3 (rs2230926) had the strongest effect related to European League Against Rheumatism response. 28639493

2017

dbSNP: rs11466657
rs11466657
0.010 GeneticVariation BEFREE I473T variant is not associated with susceptibility to RA, but it significantly correlates with erosive disease in patients seropositive for antibodies to citrullinated protein antigens (p = 0.017 in the total cohort and p = 0.0049 in female patients) and with a lower response to infliximab treatment as measured by the change in Disease Activity Score in 28 joints (p = 0.012) and by the European League Against Rheumatism criteria (p = 0.049). 27716427

2016

dbSNP: rs12720270
rs12720270
0.010 GeneticVariation BEFREE However, no associations were found between the rs12720270, rs280500, rs280523 and rs8108236 polymorphisms and susceptibility to rheumatic diseases. 26980740

2016

dbSNP: rs12720356
rs12720356
0.010 GeneticVariation BEFREE This meta-analysis demonstrates that the TYK2 rs2304256 and rs12720356 polymorphisms are associated with susceptibility to rheumatic diseases, rs2304256 polymorphism is associated with SLE in Caucasians, and rs280519 polymorphism is associated with SLE in Caucasians and Asians. 26980740

2016

dbSNP: rs2304256
rs2304256
0.010 GeneticVariation BEFREE This meta-analysis demonstrates that the TYK2 rs2304256 and rs12720356 polymorphisms are associated with susceptibility to rheumatic diseases, rs2304256 polymorphism is associated with SLE in Caucasians, and rs280519 polymorphism is associated with SLE in Caucasians and Asians. 26980740

2016

dbSNP: rs280500
rs280500
0.010 GeneticVariation BEFREE However, no associations were found between the rs12720270, rs280500, rs280523 and rs8108236 polymorphisms and susceptibility to rheumatic diseases. 26980740

2016

dbSNP: rs280519
rs280519
0.010 GeneticVariation BEFREE This meta-analysis demonstrates that the TYK2 rs2304256 and rs12720356 polymorphisms are associated with susceptibility to rheumatic diseases, rs2304256 polymorphism is associated with SLE in Caucasians, and rs280519 polymorphism is associated with SLE in Caucasians and Asians. 26980740

2016

dbSNP: rs280523
rs280523
0.010 GeneticVariation BEFREE However, no associations were found between the rs12720270, rs280500, rs280523 and rs8108236 polymorphisms and susceptibility to rheumatic diseases. 26980740

2016

dbSNP: rs8108236
rs8108236
0.010 GeneticVariation BEFREE However, no associations were found between the rs12720270, rs280500, rs280523 and rs8108236 polymorphisms and susceptibility to rheumatic diseases. 26980740

2016

dbSNP: rs10903323
rs10903323
0.010 GeneticVariation BEFREE A total of 1302 patients fulfilling the 1987 American College of Rheumatism classification criteria for RA were genotyped for the MSRA rs10903323 (G/A) polymorphism. 22657383

2012

dbSNP: rs774359492
rs774359492
0.010 GeneticVariation BEFREE This meta-analysis demonstrates that the FAS -670 A/G polymorphism confers susceptibility to rheumatic diseases in Asians and SLE and RA, and the FAS -1,377 G/A polymorphism is associated with SLE susceptibility. 23053964

2012

dbSNP: rs1799945
rs1799945
0.010 GeneticVariation BEFREE The C282Y and H63D allele frequencies were 4.5 and 12.8 in patients with rheumatic diseases. 15789881

2005

dbSNP: rs1800562
rs1800562
0.010 GeneticVariation BEFREE The C282Y and H63D allele frequencies were 4.5 and 12.8 in patients with rheumatic diseases. 15789881

2005

dbSNP: rs1799983
rs1799983
0.010 GeneticVariation BEFREE To assess potential associations between Korean Behçet's disease (BD) or other rheumatic diseases with vasculitis and two polymorphisms of the endothelial nitric oxide synthase (eNOS) gene, which include the Glu298Asp polymorphism in exon 7 and a variable number of tandem repeats (VNTR) polymorphism in intron 4. 14583572

2003