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rs1862513 |
SNP |
PedAM |
snpId=rs1862513; pubmedId=21345288; geneId=56729; geneSymbol=RETN; diseaseId=umls:C0003873; sourceId=BeFree; sentence=RETN rs1862513 polymorphism does not seem to be a genetic risk factor for both clinically evident CV disease and subclinical atherosclerosis in patients with RA.; score=0.005991584; Year=2011; geneSymbol_dbSNP=RETN; CHROMOSOME=19; POS=7668907; REF=C; ALT=G |
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rs1863800 |
SNP |
PedAM |
snpId=rs1863800; pubmedId=15022315; geneId=348120; geneSymbol=LINC01193; diseaseId=umls:C0003873; sourceId=BeFree; sentence=For the SNPs CT60 and rs1863800, unrelated patients with RA (n = 759) were compared with controls (n = 755).; score=0.001085767; Year=2004; geneSymbol_dbSNP=NA; CHROMOSOME=2; POS=203837937; REF=C; ALT=T |
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rs187084 |
SNP |
PedAM |
snpId=rs187084; pubmedId=23420357; geneId=54106; geneSymbol=TLR9; diseaseId=umls:C0003873; sourceId=BeFree; sentence=One Turkish study showed a significant difference between TLR9 rs187084 allele frequencies and rheumatoid arthritis patients and controls, while another study revealed a significant association between rheumatoid factor and TLR8 rs5741883.; score=0.003724241; Year=2013; geneSymbol_dbSNP=TLR9; CHROMOSOME=3; POS=52227015; REF=A; ALT=G |
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rs187084 |
SNP |
PedAM |
snpId=rs187084; pubmedId=23325096; geneId=54106; geneSymbol=TLR9; diseaseId=umls:C0003873; sourceId=BeFree; sentence=A significant difference between TLR9 rs187084 allele frequencies in RA patients and controls was found in one Turkish study (p = 0.003), and a moderate association between RF positivity and TLR8 rs5741883 was found in an European study (p = 0.001).; score=0.003724241; Year=2013; geneSymbol_dbSNP=TLR9; CHROMOSOME=3; POS=52227015; REF=A; ALT=G |
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rs187084 |
SNP |
PedAM |
snpId=rs187084; pubmedId=20422193; geneId=54106; geneSymbol=TLR9; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Our study suggests that a single nucleotide polymorphism (rs187084) in TLR9 gene may be a susceptibility factor for RA in Turkish population.; score=0.003724241; Year=2011; geneSymbol_dbSNP=TLR9; CHROMOSOME=3; POS=52227015; REF=A; ALT=G |
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rs1878406 |
SNP |
PedAM |
snpId=rs1878406; pubmedId=24795506; geneId=1909; geneSymbol=EDNRA; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Our results do not confirm association between ABO rs579459, PPAP2B rs17114036, ADAMTS7 rs3825807, PIK3CG rs17398575, and EDNRA rs1878406 and subclinical atherosclerosis and CV disease in RA.; score=0.000814326; Year=2014; geneSymbol_dbSNP=NA; CHROMOSOME=4; POS=147472512; REF=C; ALT=G,T |
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rs1883832 |
SNP |
PedAM |
snpId=rs1883832; pubmedId=23166616; geneId=49; geneSymbol=ACR; diseaseId=umls:C0003873; sourceId=BeFree; sentence=One thousand five hundred and seventy-five patients fulfilling the 1987 ACR classification criteria for RA and 1600 matched controls were genotyped for the CD40 rs1883832, rs4810485 and rs1535045 and CD154 rs3092952 and rs3092920 gene polymorphisms, using predesigned TaqMan single nucleotide polymorphism genotyping assays.; score=0.005700279; Year=2012; geneSymbol_dbSNP=CD40; CHROMOSOME=20; POS=46118343; REF=T; ALT=C |
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rs1883832 |
SNP |
PedAM |
snpId=rs1883832; pubmedId=23166616; geneId=958; geneSymbol=CD40; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Data from our pilot study indicate a potential association of rs1883832 CD40 gene polymorphism with susceptibility to RA.; score=0.277186332; Year=2012; geneSymbol_dbSNP=CD40; CHROMOSOME=20; POS=46118343; REF=T; ALT=C |
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rs1893592 |
SNP |
PedAM |
snpId=rs1893592; pubmedId=24390342; geneId=53347; geneSymbol=UBASH3A; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Genetics of rheumatoid arthritis contributes to biology and drug discovery.; score=0.122367032; Year=2013; geneSymbol_dbSNP=UBASH3A; CHROMOSOME=21; POS=42434957; REF=A; ALT=C |
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rs1898036 |
SNP |
PedAM |
snpId=rs1898036; pubmedId=22491018; geneId=89978; geneSymbol=DPH6; diseaseId=umls:C0003873; sourceId=GAD; sentence=[Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.]; score=0.002367032; Year=2013; geneSymbol_dbSNP=NA; CHROMOSOME=15; POS=36057645; REF=T; ALT=C |
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rs1914816 |
SNP |
PedAM |
snpId=rs1914816; pubmedId=22491018; geneId=2108; geneSymbol=ETFA; diseaseId=umls:C0003873; sourceId=GAD; sentence=[Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.]; score=0.002367032; Year=2013; geneSymbol_dbSNP=ETFA; CHROMOSOME=15; POS=76254592; REF=G; ALT=A |
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rs1950897 |
SNP |
PedAM |
snpId=rs1950897; pubmedId=24390342; geneId=5890; geneSymbol=RAD51B; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Genetics of rheumatoid arthritis contributes to biology and drug discovery.; score=0.120271442; Year=2013; geneSymbol_dbSNP=RAD51B; CHROMOSOME=14; POS=68293424; REF=C; ALT=T |
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rs1957895 |
SNP |
PedAM |
snpId=rs1957895; pubmedId=22446963; geneId=5583; geneSymbol=PRKCH; diseaseId=umls:C0003873; sourceId=GAD; sentence=[Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population.]; score=0.13309268; Year=2012; geneSymbol_dbSNP=PRKCH; CHROMOSOME=14; POS=61441614; REF=G; ALT=T |
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rs1957895 |
SNP |
PedAM |
snpId=rs1957895; pubmedId=22446963; geneId=5583; geneSymbol=PRKCH; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population.; score=0.13309268; Year=2012; geneSymbol_dbSNP=PRKCH; CHROMOSOME=14; POS=61441614; REF=G; ALT=T |
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rs1990760 |
SNP |
PedAM |
snpId=rs1990760; pubmedId=17442111; geneId=64135; geneSymbol=IFIH1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=These results indicate that the IFIH1 is upregulated in RA but that the A946T variant does not contribute significantly to the genetic background of RA.; score=0.000814326; Year=2007; geneSymbol_dbSNP=IFIH1; CHROMOSOME=2; POS=162267541; REF=C; ALT=T |
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rs1990760 |
SNP |
PedAM |
snpId=rs1990760; pubmedId=23734776; geneId=64135; geneSymbol=IFIH1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=This meta-analysis demonstrates that the IFIH1 rs1990760 T-allele confers susceptibility to T1D, SLE, MS and RA and suggests that the IFIH1 rs1990760 polymorphism might have no effect on GD and AAD.; score=0.000814326; Year=2014; geneSymbol_dbSNP=IFIH1; CHROMOSOME=2; POS=162267541; REF=C; ALT=T |
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rs199476059 |
SNP |
PedAM |
snpId=rs199476059; pubmedId=17875550; geneId=4261; geneSymbol=CIITA; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The MHC2TA -168A/G polymorphism and risk for rheumatoid arthritis: a meta-analysis of 6861 patients and 9270 controls reveals no evidence for association.; score=0.252539865; Year=2008; geneSymbol_dbSNP=CIITA;LOC105371080; CHROMOSOME=16; POS=10877163; REF=G; ALT=A |
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rs200215055 |
SNP |
PedAM |
snpId=rs200215055; 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=FCGR3B; CHROMOSOME=1; POS=161626196; REF=C; ALT=A,G |
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rs2002842 |
SNP |
PedAM |
snpId=rs2002842; pubmedId=18668548; geneId=27164; geneSymbol=SALL3; diseaseId=umls:C0003873; sourceId=GAD; sentence=[Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility.]; score=0.002367032; Year=2008; geneSymbol_dbSNP=NA; CHROMOSOME=18; POS=78649597; REF=C; ALT=A |
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rs2004640 |
SNP |
PedAM |
snpId=rs2004640; pubmedId=18843785; geneId=144125; geneSymbol=OR2AG1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Two of the IRF5 polymorphisms, CGGGGindel (OR 1.38, 95% CI 1.09-1.76, pcorr = 0.04) and rs2004640 (OR 1.36, 95% CI 1.09-1.68, pcorr = 0.03), and one haplotype, including the rs2004640 and the CGGGGindel, ht3 (A-Del-T-C-del-A-T) (OR 1.39, 95% CI 1.09-1.79, pcorr = 0.04) were significantly associated with an increased risk of RA.; score=0.000271442; Year=2008; geneSymbol_dbSNP=IRF5; CHROMOSOME=7; POS=128938247; REF=T; ALT=G |
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