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rs10181656 |
SNP |
PedAM |
snpId=rs10181656; pubmedId=22753649; geneId=6775; geneSymbol=STAT4; diseaseId=umls:C0003873; sourceId=BeFree; sentence=In addition, rs7574865 and rs10181656, in STAT4, were associated with ACPA-positive RA in the Swedish study.; score=0.316739695; Year=2012; geneSymbol_dbSNP=STAT4; CHROMOSOME=2; POS=191105153; REF=G; ALT=C |
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rs1042522 |
SNP |
PedAM |
snpId=rs1042522; pubmedId=19772793; geneId=4193; geneSymbol=MDM2; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Association of rheumatoid arthritis with Mdm2 SNP309 and genetic evidence for an allele-specific interaction between MDM2 and p53 P72R variants: a case control study.; score=0.005634266; Year=2009; geneSymbol_dbSNP=TP53; CHROMOSOME=17; POS=7676154; REF=G; ALT=T,C |
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rs1042522 |
SNP |
PedAM |
snpId=rs1042522; pubmedId=19772793; geneId=7157; geneSymbol=TP53; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Association of rheumatoid arthritis with Mdm2 SNP309 and genetic evidence for an allele-specific interaction between MDM2 and p53 P72R variants: a case control study.; score=0.030951762; Year=2009; geneSymbol_dbSNP=TP53; CHROMOSOME=17; POS=7676154; REF=G; ALT=T,C |
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rs1043099 |
SNP |
PedAM |
snpId=rs1043099; pubmedId=24449572; geneId=652968; geneSymbol=GATSL3; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study.; score=0.12; Year=2013; geneSymbol_dbSNP=GATSL3; CHROMOSOME=22; POS=30285268; REF=C; ALT=T,G |
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rs1045642 |
SNP |
PedAM |
snpId=rs1045642; pubmedId=23095111; geneId=5243; geneSymbol=ABCB1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=These data suggest that the presence of the MTHFR C677T and ABCB1 C3435T SNPs contribute to MTX toxicity in patients with RA.; score=0.134278137; Year=2012; geneSymbol_dbSNP=ABCB1; CHROMOSOME=7; POS=87509329; REF=A; ALT=T,G |
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rs1045642 |
SNP |
PedAM |
snpId=rs1045642; pubmedId=23095111; geneId=4524; geneSymbol=MTHFR; diseaseId=umls:C0003873; sourceId=BeFree; sentence=These data suggest that the presence of the MTHFR C677T and ABCB1 C3435T SNPs contribute to MTX toxicity in patients with RA.; score=0.20430773; Year=2012; geneSymbol_dbSNP=ABCB1; CHROMOSOME=7; POS=87509329; REF=A; ALT=T,G |
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rs1045642 |
SNP |
PedAM |
snpId=rs1045642; pubmedId=17181924; geneId=5243; geneSymbol=ABCB1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=ABCB1 C3435T polymorphism influences methotrexate sensitivity in rheumatoid arthritis patients.; score=0.134278137; Year=2006; geneSymbol_dbSNP=ABCB1; CHROMOSOME=7; POS=87509329; REF=A; ALT=T,G |
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rs10468473 |
SNP |
PedAM |
snpId=rs10468473; pubmedId=25732927; geneId=3123; geneSymbol=HLA-DRB1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Our data suggest a genetic interaction between MAP2K4 and HLA-DRB1, and the importance of rs10468473 and MAP2K4 splice variants in the development of autoantibody-positive RA.; score=0.36; Year=2015; geneSymbol_dbSNP=NA; CHROMOSOME=17; POS=12224359; REF=T; ALT=C |
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rs10488631 |
SNP |
PedAM |
snpId=rs10488631; pubmedId=20453842; geneId=3663; geneSymbol=IRF5; diseaseId=umls:C0003873; sourceId=GAD; sentence=[Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.]; score=0.282449467; Year=2010; geneSymbol_dbSNP=TNPO3; CHROMOSOME=7; POS=128954129; REF=T; ALT=C |
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rs10488631 |
SNP |
PedAM |
snpId=rs10488631; pubmedId=21807777; geneId=3663; geneSymbol=IRF5; diseaseId=umls:C0003873; sourceId=BeFree; sentence=One insertion-deletion polymorphism (CGGGG indel) and one single-nucleotide polymorphism (rs10488631) in the IRF5 gene were genotyped and analyzed within RA subgroups stratified by rheumatoid factor (RF) and anticitrullinated peptide antibodies (ACPA).; score=0.282449467; Year=2011; geneSymbol_dbSNP=TNPO3; CHROMOSOME=7; POS=128954129; REF=T; ALT=C |
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rs10488631 |
SNP |
PedAM |
snpId=rs10488631; pubmedId=20453842; geneId=23534; geneSymbol=TNPO3; diseaseId=umls:C0003873; sourceId=GAD; sentence=[Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.]; score=0.122367032; Year=2010; geneSymbol_dbSNP=TNPO3; CHROMOSOME=7; POS=128954129; REF=T; ALT=C |
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rs10488631 |
SNP |
PedAM |
snpId=rs10488631; pubmedId=20453842; geneId=23534; geneSymbol=TNPO3; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.; score=0.122367032; Year=2010; geneSymbol_dbSNP=TNPO3; CHROMOSOME=7; POS=128954129; REF=T; ALT=C |
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rs104895271 |
SNP |
PedAM |
snpId=rs104895271; pubmedId=23322460; geneId=7124; geneSymbol=TNF; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Symptoms related to tumor necrosis factor receptor 1-associated periodic syndrome, multiple sclerosis, and severe rheumatoid arthritis in patients carrying the TNF receptor superfamily 1A D12E/p.Asp41Glu mutation.; score=0.425384406; Year=2013; geneSymbol_dbSNP=TNFRSF1A; CHROMOSOME=12; POS=6334161; REF=A; ALT=G,C |
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rs10489629 |
SNP |
PedAM |
snpId=rs10489629; pubmedId=22718508; geneId=149233; geneSymbol=IL23R; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Association of interleukin 23 receptor gene polymorphisms (rs10489629, rs7517847) with rheumatoid arthritis in European population: a meta-analysis.; score=0.012811307; Year=2012; geneSymbol_dbSNP=IL23R; CHROMOSOME=1; POS=67222666; REF=T; ALT=C |
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rs10499194 |
SNP |
PedAM |
snpId=rs10499194; pubmedId=17982456; geneId=7128; geneSymbol=TNFAIP3; diseaseId=umls:C0003873; sourceId=BeFree; sentence=After evaluating and adjusting for technical and population biases, we identified a SNP at 6q23 (rs10499194, approximately 150 kb from TNFAIP3 and OLIG3) that was reproducibly associated with rheumatoid arthritis both in the genome-wide association (GWA) scan and in 5,541 additional case-control samples (P = 10(-3), GWA scan; P < 10(-6), replication; P = 10(-9), combined).; score=0.167568474; Year=2007; geneSymbol_dbSNP=NA; CHROMOSOME=6; POS=137681500; REF=C; ALT=T |
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rs10499194 |
SNP |
PedAM |
snpId=rs10499194; pubmedId=23450725; geneId=6775; geneSymbol=STAT4; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Childhood-onset RA was associated with TNFAIP3 rs10499194 (OR 0.60 [95% confidence interval 0.44-0.83]), PTPN22 rs2476601 (OR 1.61 [95% confidence interval 1.11-2.31]), and STAT4 rs7574865 (OR 1.41 [95% confidence interval 1.06-1.87]) variants.; score=0.316739695; Year=2013; geneSymbol_dbSNP=NA; CHROMOSOME=6; POS=137681500; REF=C; ALT=T |
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rs10499194 |
SNP |
PedAM |
snpId=rs10499194; pubmedId=17982456; geneId=167826; geneSymbol=OLIG3; diseaseId=umls:C0003873; sourceId=BeFree; sentence=After evaluating and adjusting for technical and population biases, we identified a SNP at 6q23 (rs10499194, approximately 150 kb from TNFAIP3 and OLIG3) that was reproducibly associated with rheumatoid arthritis both in the genome-wide association (GWA) scan and in 5,541 additional case-control samples (P = 10(-3), GWA scan; P < 10(-6), replication; P = 10(-9), combined).; score=0.017383549; Year=2007; geneSymbol_dbSNP=NA; CHROMOSOME=6; POS=137681500; REF=C; ALT=T |
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rs10499194 |
SNP |
PedAM |
snpId=rs10499194; pubmedId=17982456; geneId=167826; geneSymbol=OLIG3; diseaseId=umls:C0003873; sourceId=GAD; sentence=[After evaluating and adjusting for technical and population biases, we identified a SNP at 6q23 (rs10499194, approximately 150 kb from TNFAIP3 and OLIG3) that was reproducibly associated with rheumatoid arthritis both in the genome-wide association (GWA) scan and in 5,541 additional case-control samples (P = 10(-3), GWA scan; P < 10(-6), replication; P = 10(-9), combined).]; score=0.017383549; Year=2007; geneSymbol_dbSNP=NA; CHROMOSOME=6; POS=137681500; REF=C; ALT=T |
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rs10499194 |
SNP |
PedAM |
snpId=rs10499194; pubmedId=23450725; geneId=7128; geneSymbol=TNFAIP3; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Childhood-onset RA was associated with TNFAIP3 rs10499194 (OR 0.60 [95% confidence interval 0.44-0.83]), PTPN22 rs2476601 (OR 1.61 [95% confidence interval 1.11-2.31]), and STAT4 rs7574865 (OR 1.41 [95% confidence interval 1.06-1.87]) variants.; score=0.167568474; Year=2013; geneSymbol_dbSNP=NA; CHROMOSOME=6; POS=137681500; REF=C; ALT=T |
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rs10499194 |
SNP |
PedAM |
snpId=rs10499194; pubmedId=19445664; geneId=167826; geneSymbol=OLIG3; diseaseId=umls:C0003873; sourceId=GAD; sentence=[Additionally, SNPs rs7574865STAT4 (P = 9.2*10-6; OR = 1.71, 95% CI = 1.35 - 2.18) and rs2476601PTPN22 (P = 9.5*10-4; OR = 1.67, 95% CI = 1.23 - 2.26) were associated with susceptibility to RA, whereas after permutation testing OLIG3/TNFAIP3 SNPs rs10499194 and rs6920220 missed our criteria for significance (Pcorr = 0.114 and Pcorr = 0.180, respectively).]; score=0.017383549; Year=2009; geneSymbol_dbSNP=NA; CHROMOSOME=6; POS=137681500; REF=C; ALT=T |
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