Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519090
rs1057519090
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057523354
rs1057523354
A 0.700 CausalMutation CLINVAR

dbSNP: rs28936375
rs28936375
A 0.700 CausalMutation CLINVAR

dbSNP: rs540558
rs540558
0.010 GeneticVariation BEFREE 94.38% of SLE patients with arthritis were belonged to the -1687C/C (rs540558) genotype. 24219225

2014

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

2000

dbSNP: rs61752717
rs61752717
0.100 GeneticVariation BEFREE Arthritis patterns in familial Mediterranean fever patients and association with M694V mutation. 20845072

2011

dbSNP: rs104895094
rs104895094
0.010 GeneticVariation BEFREE Arthritis was high in K695R heterozygous genotype. 28483595

2017

dbSNP: rs61752717
rs61752717
0.100 GeneticVariation BEFREE M694V genotype seems to be more frequently associated with arthritis as well as with chronic arthritis than other genotypes. 28828621

2018

dbSNP: rs17197936
rs17197936
0.010 GeneticVariation BEFREE A harmful association was observed between the minor allele of rs17197936 and 2 clinical traits, count of joints with active arthritis and count of joints with pain on motion/tenderness, in patients with extended oligoarthritis. 25236364

2014

dbSNP: rs4986790
rs4986790
0.010 GeneticVariation BEFREE A phenotypic correlation of Asp299Gly-AG genotype with arthritis in UC patients was detected (P = 0.003). 29055077

2017

dbSNP: rs771184127
rs771184127
0.010 GeneticVariation BEFREE A phenotypic correlation of Asp299Gly-AG genotype with arthritis in UC patients was detected (P = 0.003). 29055077

2017

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 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 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: rs3789604
rs3789604
0.010 GeneticVariation BEFREE A total of 667 RA patients and 286 controls were genotyped for 13 PTPN22 single nucleotide polymorphisms (SNPs) by allele-specific kinetic polymerase chain reaction. rs3789604 was genotyped in an additional 410 RA and 270 UA patients participating in the Leiden early arthritis inception cohort. 17135225

2007

dbSNP: rs1800562
rs1800562
0.080 GeneticVariation BEFREE All previously undiagnosed C282Y homozygotes (35 male, 67 female) and all HFE wild-types (131 male, 160 female) with baseline and follow-up SF concentrations <1000 microg/L were assessed for HH-associated signs and symptoms including abnormal second/third metacarpophalangeal joints (MCP2/3), raised liver enzymes, hepatomegaly, and self-reported liver disease, fatigue, diabetes mellitus, and use of arthritis medication. 20583211

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: rs1800925
rs1800925
0.010 GeneticVariation BEFREE An additional SNP, rs1800925, was genotyped only in the PsA and PsC groups. 21613309

2011

dbSNP: rs61752717
rs61752717
0.100 GeneticVariation BEFREE Arthralgia or arthritis was significantly higher in M694V carriers than in non-M694V carriers (p < 0.05). 18300119

2008

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: 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: 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: rs61752717
rs61752717
0.100 GeneticVariation BEFREE Children homozygous for the M694V mutation presented at a younger age, had a higher severity score, and more commonly had arthritis. 12508410

2003

dbSNP: rs2234693
rs2234693
0.010 GeneticVariation BEFREE Conclusions Minor allele rs2234693-C was associated with renal and cutaneous involvement, as well as the absence of arthritis, anti-ANA and anti-RNP autoantibodies. 27681518

2017

dbSNP: rs61752717
rs61752717
0.100 GeneticVariation BEFREE Fever and arthritis were determined in similar ratios to other genotypes (76% and 19%, respectively) in the M694V/M694V genotype (74% and 29%, respectively) (p > 0.50 and p > 0.20, respectively). 20373849

2010