|
rs3911238 |
SNP |
PedAM |
snpId=rs3911238; pubmedId=25150077; geneId=3685; geneSymbol=ITGAV; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The ITGAV-rs3911238 polymorphism is associated with disease activity in rheumatoid arthritis.; score=0.008815624; Year=2013; geneSymbol_dbSNP=ITGAV; CHROMOSOME=2; POS=186605617; REF=G; ALT=C |
details
|
|
|
rs394581 |
SNP |
PedAM |
snpId=rs394581; pubmedId=21120996; geneId=7128; geneSymbol=TNFAIP3; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Conversely, 3 of the 27 SNPs (CCR6 rs3093023, TAGAP rs394581, and TNFAIP3 rs6920220) demonstrated ORs in the opposite direction from those reported for RA patients of European ancestry.; score=0.167568474; Year=2010; geneSymbol_dbSNP=NA; CHROMOSOME=6; POS=159061489; REF=C; ALT=T |
details
|
|
|
rs396991 |
SNP |
PedAM |
snpId=rs396991; pubmedId=26314337; geneId=1191; geneSymbol=CLU; diseaseId=umls:C0003873; sourceId=BeFree; sentence=We conducted a meta-analysis on the association between FCGR2A H131R (rs1801274), FCGR3A F158V (rs396991), and FCGR3B NA1/NA2 polymorphisms and RA susceptibility.; score=0.00408156; Year=2015; geneSymbol_dbSNP=FCGR3A; CHROMOSOME=1; POS=161544752; REF=A; ALT=G,C |
details
|
|
|
rs396991 |
SNP |
PedAM |
snpId=rs396991; pubmedId=18565259; geneId=7133; geneSymbol=TNFRSF1B; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Influence of FCGR3A-V212F and TNFRSF1B-M196R genotypes in patients with rheumatoid arthritis treated with infliximab therapy.; score=0.073283014; Year=2008; geneSymbol_dbSNP=FCGR3A; CHROMOSOME=1; POS=161544752; REF=A; ALT=G,C |
details
|
|
|
rs396991 |
SNP |
PedAM |
snpId=rs396991; pubmedId=18565259; geneId=2214; geneSymbol=FCGR3A; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Influence of FCGR3A-V212F and TNFRSF1B-M196R genotypes in patients with rheumatoid arthritis treated with infliximab therapy.; score=0.062385613; Year=2008; geneSymbol_dbSNP=FCGR3A; CHROMOSOME=1; POS=161544752; REF=A; ALT=G,C |
details
|
|
|
rs397507444 |
SNP |
PedAM |
snpId=rs397507444; pubmedId=17985847; geneId=4524; geneSymbol=MTHFR; diseaseId=umls:C0003873; sourceId=BeFree; sentence=In this study, the six polymorphisms associated with rheumatoid arthritis (RA), N-acetyltransferase2 (NAT2) gene polymorphisms T341C, G590A, and G857A, methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms C677T and A1298C, and serum amyloid A1 (SAA1) gene promoter polymorphism C-13T were simultaneously detected by the electrochemical DNA chip and the loop-mediated isothermal amplification (LAMP) method, which is a novel technique for DNA amplification.; score=0.20430773; Year=2007; geneSymbol_dbSNP=MTHFR; CHROMOSOME=1; POS=11794407; REF=T; ALT=G |
details
|
|
|
rs397507444 |
SNP |
PedAM |
snpId=rs397507444; pubmedId=15361376; geneId=4524; geneSymbol=MTHFR; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Methotrexate related adverse effects in patients with rheumatoid arthritis are associated with the A1298C polymorphism of the MTHFR gene.; score=0.20430773; Year=2004; geneSymbol_dbSNP=MTHFR; CHROMOSOME=1; POS=11794407; REF=T; ALT=G |
details
|
|
|
rs397507444 |
SNP |
PedAM |
snpId=rs397507444; pubmedId=20067328; geneId=4524; geneSymbol=MTHFR; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Associations between the C677T and A1298C polymorphisms of MTHFR and the efficacy and toxicity of methotrexate in rheumatoid arthritis: a meta-analysis.; score=0.20430773; Year=2010; geneSymbol_dbSNP=MTHFR; CHROMOSOME=1; POS=11794407; REF=T; ALT=G |
details
|
|
|
rs397507444 |
SNP |
PedAM |
snpId=rs397507444; pubmedId=20423475; geneId=4524; geneSymbol=MTHFR; diseaseId=umls:C0003873; sourceId=BeFree; sentence=A1298C polymorphism in the MTHFR gene predisposes to cardiovascular risk in rheumatoid arthritis.; score=0.20430773; Year=2010; geneSymbol_dbSNP=MTHFR; CHROMOSOME=1; POS=11794407; REF=T; ALT=G |
details
|
|
|
rs397507444 |
SNP |
PedAM |
snpId=rs397507444; pubmedId=24794492; geneId=4524; geneSymbol=MTHFR; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Association of the MTHFR C677T and A1298C polymorphisms with methotrexate toxicity in rheumatoid arthritis: a meta-analysis.; score=0.20430773; Year=2014; geneSymbol_dbSNP=MTHFR; CHROMOSOME=1; POS=11794407; REF=T; ALT=G |
details
|
|
|
rs397507444 |
SNP |
PedAM |
snpId=rs397507444; pubmedId=20514079; geneId=4524; geneSymbol=MTHFR; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Polymorphisms C677T and A1298C in the MTHFR gene in Mexican patients with rheumatoid arthritis treated with methotrexate: implication with elevation of transaminases.; score=0.20430773; Year=2011; geneSymbol_dbSNP=MTHFR; CHROMOSOME=1; POS=11794407; REF=T; ALT=G |
details
|
|
|
rs397507444 |
SNP |
PedAM |
snpId=rs397507444; pubmedId=17985847; geneId=10; geneSymbol=NAT2; diseaseId=umls:C0003873; sourceId=BeFree; sentence=In this study, the six polymorphisms associated with rheumatoid arthritis (RA), N-acetyltransferase2 (NAT2) gene polymorphisms T341C, G590A, and G857A, methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms C677T and A1298C, and serum amyloid A1 (SAA1) gene promoter polymorphism C-13T were simultaneously detected by the electrochemical DNA chip and the loop-mediated isothermal amplification (LAMP) method, which is a novel technique for DNA amplification.; score=0.019726837; Year=2007; geneSymbol_dbSNP=MTHFR; CHROMOSOME=1; POS=11794407; REF=T; ALT=G |
details
|
|
|
rs397507444 |
SNP |
PedAM |
snpId=rs397507444; pubmedId=21773884; geneId=4524; geneSymbol=MTHFR; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Methylenetetrahydrofolate reductase polymorphisms, C677T and A1298C, are associated with methotrexate-related toxicities in Korean patients with rheumatoid arthritis.; score=0.20430773; Year=2012; geneSymbol_dbSNP=MTHFR; CHROMOSOME=1; POS=11794407; REF=T; ALT=G |
details
|
|
|
rs397507444 |
SNP |
PedAM |
snpId=rs397507444; pubmedId=21931346; geneId=4524; geneSymbol=MTHFR; diseaseId=umls:C0003873; sourceId=BeFree; sentence=MTHFR gene polymorphisms and outcome of methotrexate treatment in patients with rheumatoid arthritis: analysis of key polymorphisms and meta-analysis of C677T and A1298C polymorphisms.; score=0.20430773; Year=2013; geneSymbol_dbSNP=MTHFR; CHROMOSOME=1; POS=11794407; REF=T; ALT=G |
details
|
|
|
rs397507444 |
SNP |
PedAM |
snpId=rs397507444; pubmedId=17985847; geneId=6288; geneSymbol=SAA1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=In this study, the six polymorphisms associated with rheumatoid arthritis (RA), N-acetyltransferase2 (NAT2) gene polymorphisms T341C, G590A, and G857A, methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms C677T and A1298C, and serum amyloid A1 (SAA1) gene promoter polymorphism C-13T were simultaneously detected by the electrochemical DNA chip and the loop-mediated isothermal amplification (LAMP) method, which is a novel technique for DNA amplification.; score=0.016425927; Year=2007; geneSymbol_dbSNP=MTHFR; CHROMOSOME=1; POS=11794407; REF=T; ALT=G |
details
|
|
|
rs41322052 |
SNP |
PedAM |
snpId=rs41322052; pubmedId=26314610; geneId=4846; geneSymbol=NOS3; diseaseId=umls:C0003873; sourceId=BeFree; sentence=We investigated the association of the T-786C single nucleotide polymorphism (SNP) of the endothelial nitric oxide synthase gene (NOS3), which is characterised by reduced expression of the enzyme in response to shear stress or interleukin-10 stimulation and significantly associated with coronary heart disease or rheumatoid arthritis, with the occurrence of isolated polymyalgia rheumatica.; score=0.014006695; Year=2015; geneSymbol_dbSNP=NOS3; CHROMOSOME=7; POS=150993018; REF=C; ALT=T |
details
|
|
|
rs41322052 |
SNP |
PedAM |
snpId=rs41322052; pubmedId=23481632; geneId=4846; geneSymbol=NOS3; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The purpose of this study was to analyse the effect of the T-786C polymorphism and intron 4 27 bp variable number tandem repeat(VNTR) eNOS markers for their potential association with Systemic Lupus Erythematosus(SLE), Hashimotos thyroiditis(HT) and Rheumatoid arthritis(RA) as well as to explore their effect on eNOS mRNA expression and nitrate production(NOx).; score=0.014006695; Year=2013; geneSymbol_dbSNP=NOS3; CHROMOSOME=7; POS=150993018; REF=C; ALT=T |
details
|
|
|
rs41322052 |
SNP |
PedAM |
snpId=rs41322052; pubmedId=18830734; geneId=4846; geneSymbol=NOS3; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Endothelial nitric oxide synthase T-786C polymorphism in rheumatoid arthritis: association with extraarticular manifestations.; score=0.014006695; Year=2009; geneSymbol_dbSNP=NOS3; CHROMOSOME=7; POS=150993018; REF=C; ALT=T |
details
|
|
|
rs41322052 |
SNP |
PedAM |
snpId=rs41322052; pubmedId=26314610; geneId=3586; geneSymbol=IL10; diseaseId=umls:C0003873; sourceId=BeFree; sentence=We investigated the association of the T-786C single nucleotide polymorphism (SNP) of the endothelial nitric oxide synthase gene (NOS3), which is characterised by reduced expression of the enzyme in response to shear stress or interleukin-10 stimulation and significantly associated with coronary heart disease or rheumatoid arthritis, with the occurrence of isolated polymyalgia rheumatica.; score=0.203492066; Year=2015; geneSymbol_dbSNP=NOS3; CHROMOSOME=7; POS=150993018; REF=C; ALT=T |
details
|
|
|
rs41322052 |
SNP |
PedAM |
snpId=rs41322052; pubmedId=17009241; geneId=4846; geneSymbol=NOS3; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The -786C/T single-nucleotide polymorphism in the promoter of the gene for endothelial nitric oxide synthase: insensitivity to physiologic stimuli as a risk factor for rheumatoid arthritis.; score=0.014006695; Year=2006; geneSymbol_dbSNP=NOS3; CHROMOSOME=7; POS=150993018; REF=C; ALT=T |
details
|
|
