Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs755622
rs755622
0.030 GeneticVariation BEFREE A second MIF promoter polymorphism comprises a G-to-C single nucleotide polymorphism (SNP) at position -173 (rs755622), which is in strong linkage disequilibrium with -794 7-CATT and is associated with arthritis clinical severity and higher serum and synovial fluid MIF levels. 31745872

2020

dbSNP: rs755622
rs755622
0.030 GeneticVariation BEFREE Single nucleotide polymorphism (SNP) -173 G/C (rs755622) on <i>MIF</i> gene has been associated with numerous diseases, such as arthritis and cancer. 29545822

2018

dbSNP: rs755622
rs755622
0.030 GeneticVariation BEFREE A significantly lower frequency of the G allele of rs755622 was observed in the oral aphthae, genital ulceration, hypopyon, and arthritis subgroups compared with controls (P(c) < 0.05). 22939113

2012

dbSNP: rs11614913
rs11614913
0.020 GeneticVariation BEFREE These findings did not support the genetic association between miR-146a rs2910164 (G/C) and JRA susceptibility, as well as the association of miR-196a-2 rs11614913 (C/T), miR-146a rs2431697, miR-146a rs57095329, miR-149 rs22928323 with arthritis. 31235484

2019

dbSNP: rs28940580
rs28940580
0.020 GeneticVariation BEFREE Their parents were heterozygous for the same mutation p.M680I, however, the mother showed severe symptoms of FMF (recurrent attacks of fever, arthralgia and arthritis, abdominal pain, thoracic pain), the father showed recurrent pustulosis prevalent on the hands and limbs, with arthralgia and abdominal pain. 31443670

2019

dbSNP: rs2910164
rs2910164
0.020 GeneticVariation BEFREE But, we also find miRNA-146 rs2910164 and miRNA-499 rs3746444 polymorphism are associated with inflammatory arthritis in Middle East. 31223622

2019

dbSNP: rs2910164
rs2910164
0.020 GeneticVariation BEFREE These findings did not support the genetic association between miR-146a rs2910164 (G/C) and JRA susceptibility, as well as the association of miR-196a-2 rs11614913 (C/T), miR-146a rs2431697, miR-146a rs57095329, miR-149 rs22928323 with arthritis. 31235484

2019

dbSNP: rs204989
rs204989
0.020 GeneticVariation BEFREE GPSM3 deficiency protects mice from inflammatory arthritis and, in humans, GPSM3 single-nucleotide polymorphisms (SNPs) are inversely associated with the risk of rheumatoid arthritis development; recently, these polymorphisms were linked to one particular SNP (rs204989) that decreases GPSM3 transcript abundance. 27307211

2016

dbSNP: rs204989
rs204989
0.020 GeneticVariation BEFREE Previous genome-wide association studies have highlighted single-nucleotide polymorphisms (SNPs; rs204989 and rs204991) in a region upstream of the GPSM3 transcription start site as being inversely correlated to the prevalence of rheumatoid arthritis (RA)-this association is supported by the protection afforded to Gpsm3-deficient mice in models of inflammatory arthritis. 26821282

2016

dbSNP: rs11614913
rs11614913
0.020 GeneticVariation BEFREE A stratified analysis showed an association of the rs11614913 TT genotype and T allele with the arthritis subgroup of BD (P(c) = 5.3 × 10(-3), OR = 1.89; P(c) = 0.015, OR = 1.56, respectively). 23928854

2013

dbSNP: rs3743930
rs3743930
0.020 GeneticVariation BEFREE Significant increase in abdominal pain and arthritis was found in patients with homozygote M694V mutation compared to those with E148Q mutation. 19777236

2010

dbSNP: rs3743930
rs3743930
0.020 GeneticVariation BEFREE Although four of the 26 patients with E148Q/E148Q were asymptomatic at the time of evaluation, abdominal pain was seen in 77% of the patients, fever in 66%, arthralgia in 50%, arthritis in 15.4%, and vomiting in 23.8%. 15458961

2005

dbSNP: rs28940580
rs28940580
0.020 GeneticVariation BEFREE Arthritis frequency was found to be lower in the patients with homozygous Met680Ile mutation. 10662876

2000

dbSNP: rs11747270
rs11747270
0.010 GeneticVariation BEFREE IRGM rs4958847 and rs11747270 increased the risk of developing arthritis in patients with CD. 31654602

2020

dbSNP: rs4958847
rs4958847
0.010 GeneticVariation BEFREE IRGM rs4958847 and rs11747270 increased the risk of developing arthritis in patients with CD. 31654602

2020

dbSNP: rs10036748
rs10036748
0.010 GeneticVariation BEFREE Patients with psoriasis with TT genotype of rs10036748 in TNIP1, with lower BMI, without arthritis will achieve a better response to MTX. 31020648

2019

dbSNP: rs1544410
rs1544410
VDR
0.010 GeneticVariation BEFREE The clinical characteristics of BD patients were evaluated and patients with ocular lesions had a higher percentage of rs1544410 A alleles (p = 0.004), and patients with oral aphthous lesions, a positive pathergy tests, and arthritis had more rs2228570 C alleles than patients without these clinical findings (respectively, p < 0.001, p = 0.021, p = 0.045). 30730049

2019

dbSNP: rs1562444
rs1562444
0.010 GeneticVariation BEFREE Case-only analysis showed associations of rs2165667 and rs1562444 with arthritis, rs10830962 with malar rash, rs3760138 with immunological abnormality, and rs8150 with hematological abnormality. 31815152

2019

dbSNP: rs2165667
rs2165667
0.010 GeneticVariation BEFREE Case-only analysis showed associations of rs2165667 and rs1562444 with arthritis, rs10830962 with malar rash, rs3760138 with immunological abnormality, and rs8150 with hematological abnormality. 31815152

2019

dbSNP: rs2228570
rs2228570
VDR
0.010 GeneticVariation BEFREE The clinical characteristics of BD patients were evaluated and patients with ocular lesions had a higher percentage of rs1544410 A alleles (p = 0.004), and patients with oral aphthous lesions, a positive pathergy tests, and arthritis had more rs2228570 C alleles than patients without these clinical findings (respectively, p < 0.001, p = 0.021, p = 0.045). 30730049

2019

dbSNP: rs224222
rs224222
0.010 GeneticVariation BEFREE Recurrent abdominal pain and arthritis/arthralgia were commonly observed in patients with M694V and R202Q mutations. 30284126

2019

dbSNP: rs2476601
rs2476601
0.010 GeneticVariation BEFREE Patients with rheumatoid arthritis (RA) or undifferentiated arthritis (UA) in the CONAART database (Argentine Consortium for Early Arthritis) were assessed for genetic risk factors for RA, specifically for HLA-DRB1 alleles and the PTPN22 rs2476601 polymorphism associated with progression to RA.This is a case-control study. 30306282

2019

dbSNP: rs3746444
rs3746444
0.010 GeneticVariation BEFREE The present study indicates that miRNA-499 rs3746444 polymorphism is associated with inflammatory arthritis susceptibility. 31223622

2019

dbSNP: rs731236
rs731236
VDR
0.010 GeneticVariation BEFREE The rs10735810, rs1544410, rs7975232, and rs731236 were associated with the onset of arthritis at both allelic and genotypic level (p < 0.01). 31011579

2019

dbSNP: rs741761
rs741761
0.010 GeneticVariation BEFREE There were differences in the genotype frequencies and allele frequencies of rs741761 between SLE patients with and without arthritis. 31394943

2019