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rs2075876 |
SNP |
PedAM |
snpId=rs2075876; pubmedId=21505073; geneId=326; geneSymbol=AIRE; diseaseId=umls:C0003873; sourceId=GAD; sentence=[The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population.]; score=0.123181358; Year=2011; geneSymbol_dbSNP=AIRE; CHROMOSOME=21; POS=44289270; REF=G; ALT=A |
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rs2075876 |
SNP |
PedAM |
snpId=rs2075876; pubmedId=21505073; geneId=326; geneSymbol=AIRE; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population.; score=0.123181358; Year=2011; geneSymbol_dbSNP=AIRE; CHROMOSOME=21; POS=44289270; REF=G; ALT=A |
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rs2075876 |
SNP |
PedAM |
snpId=rs2075876; pubmedId=25637666; geneId=326; geneSymbol=AIRE; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Association of rs2075876 polymorphism of AIRE gene with rheumatoid arthritis risk.; score=0.123181358; Year=2015; geneSymbol_dbSNP=AIRE; CHROMOSOME=21; POS=44289270; REF=G; ALT=A |
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rs2075876 |
SNP |
PedAM |
snpId=rs2075876; pubmedId=25637666; geneId=140913; geneSymbol=PPIAP10; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Furthermore, in correlation analysis of SNPs in AIRE gene with clinical characteristics of rheumatoid arthritis, we found the SNP rs2075876 had significant correlation with CRP concentration (pa=0.020).; score=0.003800186; Year=2015; geneSymbol_dbSNP=AIRE; CHROMOSOME=21; POS=44289270; REF=G; ALT=A |
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rs2075876 |
SNP |
PedAM |
snpId=rs2075876; pubmedId=21505073; geneId=5211; geneSymbol=PFKL; diseaseId=umls:C0003873; sourceId=GAD; sentence=[The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population.]; score=0.002367032; Year=2011; geneSymbol_dbSNP=AIRE; CHROMOSOME=21; POS=44289270; REF=G; ALT=A |
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rs2076530 |
SNP |
PedAM |
snpId=rs2076530; pubmedId=16690410; geneId=56244; geneSymbol=BTNL2; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The aim of this study was to test whether the functional variant rs2076530 of the BTNL2 gene confers susceptibility to the autoimmune diseases type 1 diabetes (T1D), rheumatoid arthritis (RA), and systemic lupus erythematosus (SLE).; score=0.128001298; Year=2005; geneSymbol_dbSNP=BTNL2;LOC101929163; CHROMOSOME=6; POS=32396039; REF=T; ALT=C |
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rs208294 |
SNP |
PedAM |
snpId=rs208294; pubmedId=22703695; geneId=5027; geneSymbol=P2RX7; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The His155Tyr (489C>T) single nucleotide polymorphism of P2RX7 gene confers an enhanced function of P2X7 receptor in immune cells from patients with rheumatoid arthritis.; score=0.005905708; Year=2012; geneSymbol_dbSNP=P2RX7;LOC105370032; CHROMOSOME=12; POS=121162450; REF=T; ALT=G,C,A |
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rs2104286 |
SNP |
PedAM |
snpId=rs2104286; pubmedId=24449572; geneId=3559; geneSymbol=IL2RA; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study.; score=0.256721114; Year=2013; geneSymbol_dbSNP=IL2RA; CHROMOSOME=10; POS=6057082; REF=T; ALT=C |
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rs2105325 |
SNP |
PedAM |
snpId=rs2105325; pubmedId=24390342; geneId=100506023; geneSymbol=LOC100506023; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Genetics of rheumatoid arthritis contributes to biology and drug discovery.; score=0.12; Year=2013; geneSymbol_dbSNP=LOC100506023; CHROMOSOME=1; POS=173380586; REF=A; ALT=C |
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rs2167270 |
SNP |
PedAM |
snpId=rs2167270; pubmedId=21385539; geneId=3952; geneSymbol=LEP; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Lack of association between LEP rs2167270 (19 G>A) polymorphism and disease susceptibility and cardiovascular disease in patients with rheumatoid arthritis.; score=0.003538676; Year=2011; geneSymbol_dbSNP=LEP; CHROMOSOME=7; POS=128241296; REF=G; ALT=A |
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rs2195534 |
SNP |
PedAM |
snpId=rs2195534; pubmedId=18466450; geneId=147372; geneSymbol=CCBE1; diseaseId=umls:C0003873; sourceId=GAD; sentence=[Multilocus analysis of GAW15 NARAC chromosome 18 case-control data.]; score=0.002367032; Year=2007; geneSymbol_dbSNP=CCBE1; CHROMOSOME=18; POS=59697596; REF=C; ALT=T |
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rs2206593 |
SNP |
PedAM |
snpId=rs2206593; pubmedId=20448286; geneId=5743; geneSymbol=PTGS2; diseaseId=umls:C0003873; sourceId=GAD; sentence=[Several SNPs mapping to the TLR and NFkappaB signalling systems demonstrated association with anti-TNF response as a whole and, in particular, with response to etanercept. Validation of these findings in an independent cohort is now warranted.]; score=0.136340051; Year=2010; geneSymbol_dbSNP=PTGS2; CHROMOSOME=1; POS=186673297; REF=A; ALT=G |
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rs2228044 |
SNP |
PedAM |
snpId=rs2228044; pubmedId=21981268; geneId=3572; geneSymbol=IL6ST; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Lack of association of IL6R rs2228145 and IL6ST/gp130 rs2228044 gene polymorphisms with cardiovascular disease in patients with rheumatoid arthritis.; score=0.204538567; Year=2011; geneSymbol_dbSNP=IL6ST; CHROMOSOME=5; POS=55968325; REF=C; ALT=G |
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rs2228044 |
SNP |
PedAM |
snpId=rs2228044; pubmedId=21981268; geneId=3570; geneSymbol=IL6R; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Lack of association of IL6R rs2228145 and IL6ST/gp130 rs2228044 gene polymorphisms with cardiovascular disease in patients with rheumatoid arthritis.; score=0.247719925; Year=2011; geneSymbol_dbSNP=IL6ST; CHROMOSOME=5; POS=55968325; REF=C; ALT=G |
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rs2228145 |
SNP |
PedAM |
snpId=rs2228145; pubmedId=23593036; geneId=3569; geneSymbol=IL6; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Although a common, non-synonymous variant in the IL-6 receptor gene (IL6R Asp358Ala; rs2228145 A>C) is associated with the risk of several common diseases, with the 358Ala allele conferring protection from coronary heart disease (CHD), rheumatoid arthritis (RA), atrial fibrillation (AF), abdominal aortic aneurysm (AAA), and increased susceptibility to asthma, the variant's effect on IL-6 signaling is not known.; score=0.212623944; Year=2013; geneSymbol_dbSNP=IL6R; CHROMOSOME=1; POS=154454494; REF=A; ALT=C,T |
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rs2228145 |
SNP |
PedAM |
snpId=rs2228145; pubmedId=21981268; geneId=3570; geneSymbol=IL6R; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Lack of association of IL6R rs2228145 and IL6ST/gp130 rs2228044 gene polymorphisms with cardiovascular disease in patients with rheumatoid arthritis.; score=0.247719925; Year=2011; geneSymbol_dbSNP=IL6R; CHROMOSOME=1; POS=154454494; REF=A; ALT=C,T |
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rs2228145 |
SNP |
PedAM |
snpId=rs2228145; pubmedId=21981268; geneId=3572; geneSymbol=IL6ST; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Lack of association of IL6R rs2228145 and IL6ST/gp130 rs2228044 gene polymorphisms with cardiovascular disease in patients with rheumatoid arthritis.; score=0.204538567; Year=2011; geneSymbol_dbSNP=IL6R; CHROMOSOME=1; POS=154454494; REF=A; ALT=C,T |
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rs2228145 |
SNP |
PedAM |
snpId=rs2228145; pubmedId=23593036; geneId=3570; geneSymbol=IL6R; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Although a common, non-synonymous variant in the IL-6 receptor gene (IL6R Asp358Ala; rs2228145 A>C) is associated with the risk of several common diseases, with the 358Ala allele conferring protection from coronary heart disease (CHD), rheumatoid arthritis (RA), atrial fibrillation (AF), abdominal aortic aneurysm (AAA), and increased susceptibility to asthma, the variant's effect on IL-6 signaling is not known.; score=0.247719925; Year=2013; geneSymbol_dbSNP=IL6R; CHROMOSOME=1; POS=154454494; REF=A; ALT=C,T |
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rs2228145 |
SNP |
PedAM |
snpId=rs2228145; pubmedId=24978393; geneId=3570; geneSymbol=IL6R; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Interleukin-6-receptor polymorphisms rs12083537, rs2228145, and rs4329505 as predictors of response to tocilizumab in rheumatoid arthritis.; score=0.247719925; Year=2014; geneSymbol_dbSNP=IL6R; CHROMOSOME=1; POS=154454494; REF=A; ALT=C,T |
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rs2228145 |
SNP |
PedAM |
snpId=rs2228145; pubmedId=24390342; geneId=3570; geneSymbol=IL6R; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Genetics of rheumatoid arthritis contributes to biology and drug discovery.; score=0.247719925; Year=2013; geneSymbol_dbSNP=IL6R; CHROMOSOME=1; POS=154454494; REF=A; ALT=C,T |
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