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rs2243250 |
SNP |
PedAM |
snpId=rs2243250; pubmedId=24628947; geneId=3565; geneSymbol=IL4; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The present study suggests that the IL-4 rs2243250 polymorphism might be associated with genetic susceptibility to autoimmune diseases, including RA and MS.; score=0.033418483; Year=2014; geneSymbol_dbSNP=IL4; CHROMOSOME=5; POS=132673462; REF=C; ALT=T |
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rs2248932 |
SNP |
PedAM |
snpId=rs2248932; pubmedId=22740142; geneId=140913; geneSymbol=PPIAP10; diseaseId=umls:C0003873; sourceId=BeFree; sentence=In stratification analyses, a significantly increased risk for RA associated with the BLK rs2248932 CC genotype was evident among younger patients, CRP-negative patients and anti-CCP-positive patients compared with the BLK rs2248932 TT/TC genotype.; score=0.003800186; Year=2012; geneSymbol_dbSNP=BLK; CHROMOSOME=8; POS=11534141; REF=A; ALT=G |
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rs2275913 |
SNP |
PedAM |
snpId=rs2275913; pubmedId=25387578; geneId=7124; geneSymbol=TNF; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The present study aimed to determine the association between the polymorphic variants of the IL-17A (rs2275913), IL-17F (rs763780) and IL-23R (rs11209026) genes and RA susceptibility, progression and response to therapy with TNF-¦Á inhibitors.; score=0.425384406; Year=2014; geneSymbol_dbSNP=IL17A; CHROMOSOME=6; POS=52186235; REF=G; ALT=A |
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rs2277438 |
SNP |
PedAM |
snpId=rs2277438; pubmedId=20231205; geneId=8792; geneSymbol=TNFRSF11A; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Genotype distributions of the SNP rs35211496 in the RANK gene as well as the SNP rs2277438 in the RANKL gene differed significantly between patients with RA and HC.; score=0.006634157; Year=2010; geneSymbol_dbSNP=TNFSF11; CHROMOSOME=13; POS=42581032; REF=G; ALT=A,C |
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rs2277438 |
SNP |
PedAM |
snpId=rs2277438; pubmedId=20231205; geneId=8600; geneSymbol=TNFSF11; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Genotype distributions of the SNP rs35211496 in the RANK gene as well as the SNP rs2277438 in the RANKL gene differed significantly between patients with RA and HC.; score=0.027694459; Year=2010; geneSymbol_dbSNP=TNFSF11; CHROMOSOME=13; POS=42581032; REF=G; ALT=A,C |
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rs2280381 |
SNP |
PedAM |
snpId=rs2280381; pubmedId=22446963; geneId=3394; geneSymbol=IRF8; diseaseId=umls:C0003873; sourceId=GAD; sentence=[Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population.]; score=0.122367032; Year=2012; geneSymbol_dbSNP=NA; CHROMOSOME=16; POS=85985027; REF=C; ALT=T |
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rs2301888 |
SNP |
PedAM |
snpId=rs2301888; pubmedId=24390342; geneId=23569; geneSymbol=PADI4; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Genetics of rheumatoid arthritis contributes to biology and drug discovery.; score=0.33168498; Year=2013; geneSymbol_dbSNP=PADI4; CHROMOSOME=1; POS=17346235; REF=G; ALT=A |
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rs2304256 |
SNP |
PedAM |
snpId=rs2304256; pubmedId=19714582; geneId=54899; geneSymbol=PXK; diseaseId=umls:C0003873; sourceId=BeFree; sentence=A characteristic single-nucleotide polymorphism (SNP) in each of 9 genetic factors, ITGAM (rs1143679), C8orf13-BLK (rs13277113), TYK2 (rs2304256), 1q25.1 (rs10798269), PXK (rs6445975), KIAA1542 (rs4963128), MECP2 (rs17435), BANK1 (rs17266594), and LY9 (rs509749), was studied in 1,635 patients with RA and 1,906 control subjects from Spain.; score=0.125005506; Year=2009; geneSymbol_dbSNP=TYK2; CHROMOSOME=19; POS=10364976; REF=C; ALT=A |
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rs2304256 |
SNP |
PedAM |
snpId=rs2304256; pubmedId=19714582; geneId=3684; geneSymbol=ITGAM; diseaseId=umls:C0003873; sourceId=BeFree; sentence=A characteristic single-nucleotide polymorphism (SNP) in each of 9 genetic factors, ITGAM (rs1143679), C8orf13-BLK (rs13277113), TYK2 (rs2304256), 1q25.1 (rs10798269), PXK (rs6445975), KIAA1542 (rs4963128), MECP2 (rs17435), BANK1 (rs17266594), and LY9 (rs509749), was studied in 1,635 patients with RA and 1,906 control subjects from Spain.; score=0.000814326; Year=2009; geneSymbol_dbSNP=TYK2; CHROMOSOME=19; POS=10364976; REF=C; ALT=A |
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rs2304256 |
SNP |
PedAM |
snpId=rs2304256; pubmedId=19714582; geneId=4204; geneSymbol=MECP2; diseaseId=umls:C0003873; sourceId=BeFree; sentence=A characteristic single-nucleotide polymorphism (SNP) in each of 9 genetic factors, ITGAM (rs1143679), C8orf13-BLK (rs13277113), TYK2 (rs2304256), 1q25.1 (rs10798269), PXK (rs6445975), KIAA1542 (rs4963128), MECP2 (rs17435), BANK1 (rs17266594), and LY9 (rs509749), was studied in 1,635 patients with RA and 1,906 control subjects from Spain.; score=0.120814326; Year=2009; geneSymbol_dbSNP=TYK2; CHROMOSOME=19; POS=10364976; REF=C; ALT=A |
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rs2304256 |
SNP |
PedAM |
snpId=rs2304256; pubmedId=19714582; geneId=55024; geneSymbol=BANK1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=A characteristic single-nucleotide polymorphism (SNP) in each of 9 genetic factors, ITGAM (rs1143679), C8orf13-BLK (rs13277113), TYK2 (rs2304256), 1q25.1 (rs10798269), PXK (rs6445975), KIAA1542 (rs4963128), MECP2 (rs17435), BANK1 (rs17266594), and LY9 (rs509749), was studied in 1,635 patients with RA and 1,906 control subjects from Spain.; score=0.003181358; Year=2009; geneSymbol_dbSNP=TYK2; CHROMOSOME=19; POS=10364976; REF=C; ALT=A |
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rs231775 |
SNP |
PedAM |
snpId=rs231775; pubmedId=21503616; geneId=1493; geneSymbol=CTLA4; diseaseId=umls:C0003873; sourceId=BeFree; sentence=CTLA4 exon1 A49G polymorphism in Slovak patients with rheumatoid arthritis and Hashimoto thyroiditis-results and the review of the literature.; score=0.345272224; Year=2011; geneSymbol_dbSNP=CTLA4; CHROMOSOME=2; POS=203867991; REF=A; ALT=G,T |
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rs237025 |
SNP |
PedAM |
snpId=rs237025; pubmedId=16735488; geneId=387082; geneSymbol=SUMO4; diseaseId=umls:C0003873; sourceId=BeFree; sentence=SUMO4 M55V variant was associated not only with type 1 diabetes [odds ratio (OR), 1.42; 95% confidence interval (CI), 1.09-1.84; P = 0.0072], but also with increased risk of other autoimmune diseases, AITD (OR, 1.52; 95% CI, 1.14-2.03; P = 0.0041) and RA without amyloidosis (OR, 1.53; 95% CI, 1.65-2.24; P = 0.027), but not primary Sjgren's syndrome.; score=0.005276948; Year=2006; geneSymbol_dbSNP=TAB2;SUMO4; CHROMOSOME=6; POS=149400554; REF=G; ALT=A |
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rs2372536 |
SNP |
PedAM |
snpId=rs2372536; pubmedId=15457444; geneId=6573; geneSymbol=SLC19A1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=We investigated the contribution of common genetic polymorphisms in RFC-1 (G80A), ATIC (C347G), and TS (28-bp tandem repeats located in the TS enhancer region [TSER*2/*3]) and of MTXPGs to the effect of MTX in patients with rheumatoid arthritis.; score=0.019998279; Year=2004; geneSymbol_dbSNP=ATIC; CHROMOSOME=2; POS=215325297; REF=C; ALT=G |
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rs2372536 |
SNP |
PedAM |
snpId=rs2372536; pubmedId=15457444; geneId=471; geneSymbol=ATIC; diseaseId=umls:C0003873; sourceId=BeFree; sentence=We investigated the contribution of common genetic polymorphisms in RFC-1 (G80A), ATIC (C347G), and TS (28-bp tandem repeats located in the TS enhancer region [TSER*2/*3]) and of MTXPGs to the effect of MTX in patients with rheumatoid arthritis.; score=0.137197984; Year=2004; geneSymbol_dbSNP=ATIC; CHROMOSOME=2; POS=215325297; REF=C; ALT=G |
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rs2377422 |
SNP |
PedAM |
snpId=rs2377422; pubmedId=22829930; geneId=50856; geneSymbol=CLEC4A; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Our data provide evidence for association between DCIR rs2377422 and RA in non-Caucasian populations and confirm the influence of DCIR polymorphisms on RA susceptibility, especially on ACPA-negative RA.; score=0.00408156; Year=2012; geneSymbol_dbSNP=CLEC4A; CHROMOSOME=12; POS=8128312; REF=C; ALT=T |
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rs2395106 |
SNP |
PedAM |
snpId=rs2395106; pubmedId=19143814; geneId=4855; geneSymbol=NOTCH4; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The strongest association within class III markers was with rs2395106 that maps 5' to the NOTCH4 gene, which has also been implicated in susceptibility to rheumatoid arthritis.; score=0.010825337; Year=2009; geneSymbol_dbSNP=NOTCH4; CHROMOSOME=6; POS=32225443; REF=A; ALT=G |
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rs2430561 |
SNP |
PedAM |
snpId=rs2430561; pubmedId=23077565; geneId=3458; geneSymbol=IFNG; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Analysis of the interferon gamma (rs2430561, +874T/A) functional gene variant in relation to the presence of cardiovascular events in rheumatoid arthritis.; score=0.146664774; Year=2012; geneSymbol_dbSNP=IFNG; CHROMOSOME=12; POS=68158742; REF=T; ALT=A |
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rs243865 |
SNP |
PedAM |
snpId=rs243865; pubmedId=18205826; geneId=4313; geneSymbol=MMP2; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The MMP2 rs243865-T allele is not a major genetic factor for rheumatoid arthritis in the French Caucasian population.; score=0.13261581; Year=2008; geneSymbol_dbSNP=MMP2; CHROMOSOME=16; POS=55477894; REF=C; ALT=T |
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rs2469434 |
SNP |
PedAM |
snpId=rs2469434; pubmedId=24390342; geneId=10666; geneSymbol=CD226; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Genetics of rheumatoid arthritis contributes to biology and drug discovery.; score=0.126905599; Year=2013; geneSymbol_dbSNP=CD226; CHROMOSOME=18; POS=69876810; REF=T; ALT=C |
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