Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1143679
rs1143679
0.900 GeneticVariation BEFREE A second study carried out in patients from Yucatan, a southeastern part of Mexico (with a high Amerindian ancestry), also replicated SLE association with all four SNPs, including the functional SNP, rs1143679 (OR = 24.6 and p = 9.3X10-6). 31774828

2019

dbSNP: rs2230926
rs2230926
0.900 GeneticVariation BEFREE The TT > A variants and the TNFAIP3 exon 3 coding variant rs2230926 demonstrated significant associations in SLE (P<sub>TT > A</sub> = 8.96 × 10<sup>-12</sup>, odds ratio [OR] = 2.07, 95% confidence interval [CI] = 1.68-2.55). 30529365

2019

dbSNP: rs2230926
rs2230926
0.900 GeneticVariation BEFREE A higher risk to develop SLE was observed for rs2230926 (<i>P</i> = 0.02, OR = 1.92). 31534975

2019

dbSNP: rs2476601
rs2476601
0.900 GeneticVariation GWASCAT Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases. 30573655

2019

dbSNP: rs2476601
rs2476601
0.900 GeneticVariation BEFREE Since the expression of the negative T-cell signaling molecule PTPN22 is increased and a marker of poor prognosis in SLE, we tested the influence of its missense risk allele Trp<sup>620</sup> (rs2476601C>T) on Treg frequency. 31781109

2019

dbSNP: rs2476601
rs2476601
0.900 GeneticVariation BEFREE Among the 26 non-MHC gene alleles analyzed, SNP rs2476601 in PTPN22 gene confers the highest risk for SLE (p = 0.0001; OR = 5.6). 31032751

2019

dbSNP: rs2476601
rs2476601
0.900 GeneticVariation BEFREE In observational studies, the associations of 1858 C/T genetic variant were noteworthy for 12 autoimmune or autoimmunity-related diseases (rheumatoid arthritis, systemic lupus erythematosus, type 1 diabetes mellitus, juvenile idiopathic arthritis, Crohn's disease, anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, vitiligo, Graves' disease, myasthenia gravis, Addison's disease, giant cell arteritis, and endometriosis). 30871019

2019

dbSNP: rs1143679
rs1143679
0.900 GeneticVariation BEFREE Conclusion CD11b rs</span>1143679 appears to be associated with risk for SLE in the Han Chinese population, and may play an important role in the development of lupus nephritis. 29207897

2018

dbSNP: rs1143679
rs1143679
A 0.900 GeneticVariation GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469

2017

dbSNP: rs1143679
rs1143679
0.900 GeneticVariation BEFREE We aimed to analyze three SNPs located in the <i>STAT4</i> (rs7574865), <i>ITGAM</i> (rs1143679) and <i>TNXB</i> (rs1150754) genes in both DLE and SLE patients from Poland. 28670251

2017

dbSNP: rs2476601
rs2476601
0.900 GeneticVariation GWASCAT A combined large-scale meta-analysis identifies COG6 as a novel shared risk locus for rheumatoid arthritis and systemic lupus erythematosus. 27193031

2017

dbSNP: rs2476601
rs2476601
A 0.900 GeneticVariation GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469

2017

dbSNP: rs2476601
rs2476601
0.900 GeneticVariation BEFREE PTPN22 R620W was associated with GD susceptibility (OR 4.3, p = 0.004), but was not associated with SLE (OR 1.8, p = 0.19). 28500376

2017

dbSNP: rs2476601
rs2476601
0.900 GeneticVariation BEFREE In summary, PTPN22 rs2476601 was significantly interrelated with SLE and contributed to susceptibility and development of SLE in Americans, Europeans and Africans in this analysis, while their relationship needs to be validated in Africans by future research. 28528372

2017

dbSNP: rs2476601
rs2476601
0.900 GeneticVariation BEFREE PTPN22 1858C > T polymorphism and susceptibility to systemic lupus erythematosus: a meta-analysis update. 28990435

2017

dbSNP: rs7574865
rs7574865
0.900 GeneticVariation BEFREE We aimed to analyze three SNPs located in the <i>STAT4</i> (rs7574865), <i>ITGAM</i> (rs1143679) and <i>TNXB</i> (rs1150754) genes in both DLE and SLE patients from Poland. 28670251

2017

dbSNP: rs7574865
rs7574865
0.900 GeneticVariation BEFREE STAT4 polymorphism, rs7574865 is linked to various autoimmune diseases such as systemic lupus erythematosus and rheumatoid arthritis. 27960128

2017

dbSNP: rs1143679
rs1143679
A 0.900 GeneticVariation GWASCAT Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture. 26606652

2016

dbSNP: rs1143679
rs1143679
0.900 GeneticVariation BEFREE This includes a detailed examination of molecular mechanisms that could explain the risk-conferring effect of rs1143679, a single nucleotide non-synonymous Mac-1 polymorphism associated with SLE. 26683153

2016

dbSNP: rs1143679
rs1143679
0.900 GeneticVariation GWASCAT Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. 27399966

2016

dbSNP: rs1143679
rs1143679
0.900 GeneticVariation BEFREE The R77H variant of CD11b, encoded by the ITGAM rs1143679 polymorphism, is associated robustly with development of the autoimmune disease systemic lupus erythematosus (SLE) and impairs CR3 function, including its regulatory role on monocyte immune signalling. 27118513

2016

dbSNP: rs2230926
rs2230926
0.900 GeneticVariation GWASCAT Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG16L2, FCHSD2, and P2RY2 in Koreans. 26663301

2016

dbSNP: rs2230926
rs2230926
0.900 GeneticVariation GWASCAT Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. 27399966

2016

dbSNP: rs2230926
rs2230926
0.900 GeneticVariation BEFREE The results of our meta-analysis suggest that TNFAIP3 (rs2230926, rs5029937, rs5029939, and rs3757173) polymorphisms are associated with susceptibility to SLE. 27726311

2016

dbSNP: rs2476601
rs2476601
0.900 GeneticVariation GWASCAT Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. 27399966

2016