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rs3738919 |
SNP |
PedAM |
snpId=rs3738919; pubmedId=19818132; geneId=3685; geneSymbol=ITGAV; diseaseId=umls:C0003873; sourceId=GAD; sentence=[The ITGAV rs3738919 variant and susceptibility to rheumatoid arthritis in four Caucasian sample sets.]; score=0.008815624; Year=2009; geneSymbol_dbSNP=ITGAV; CHROMOSOME=2; POS=186656533; REF=C; ALT=A |
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rs3738919 |
SNP |
PedAM |
snpId=rs3738919; pubmedId=17615072; geneId=3685; geneSymbol=ITGAV; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The ITGAV rs3738919-C allele is associated with rheumatoid arthritis in the European Caucasian population: a family-based study.; score=0.008815624; Year=2007; geneSymbol_dbSNP=ITGAV; CHROMOSOME=2; POS=186656533; REF=C; ALT=A |
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rs3738919 |
SNP |
PedAM |
snpId=rs3738919; pubmedId=19818132; geneId=3685; geneSymbol=ITGAV; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The ITGAV rs3738919 variant and susceptibility to rheumatoid arthritis in four Caucasian sample sets.; score=0.008815624; Year=2009; geneSymbol_dbSNP=ITGAV; CHROMOSOME=2; POS=186656533; REF=C; ALT=A |
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rs3746444 |
SNP |
PedAM |
snpId=rs3746444; pubmedId=23138379; geneId=574501; geneSymbol=MIR499A; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Our findings demonstrated that the hsa-mir-499 rs3746444, but not mir-146a rs2910164, polymorphism is associated with an increased RA risk in a sample of the Iranian population.; score=0.001357209; Year=2012; geneSymbol_dbSNP=MYH7B;MIR499A;MIR499B; CHROMOSOME=20; POS=34990448; REF=A; ALT=G |
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rs3746444 |
SNP |
PedAM |
snpId=rs3746444; pubmedId=23138379; geneId=406938; geneSymbol=MIR146A; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Our findings demonstrated that the hsa-mir-499 rs3746444, but not mir-146a rs2910164, polymorphism is associated with an increased RA risk in a sample of the Iranian population.; score=0.012973128; Year=2012; geneSymbol_dbSNP=MYH7B;MIR499A;MIR499B; CHROMOSOME=20; POS=34990448; REF=A; ALT=G |
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rs3746444 |
SNP |
PedAM |
snpId=rs3746444; pubmedId=22451023; geneId=574501; geneSymbol=MIR499A; diseaseId=umls:C0003873; sourceId=BeFree; sentence=However, the hsa-mir-499 rs3746444 T/C polymorphism may not be associated with susceptibility to rheumatoid arthritis.; score=0.001357209; Year=2013; geneSymbol_dbSNP=MYH7B;MIR499A;MIR499B; CHROMOSOME=20; POS=34990448; REF=A; ALT=G |
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rs3746444 |
SNP |
PedAM |
snpId=rs3746444; pubmedId=21181275; geneId=406938; geneSymbol=MIR146A; diseaseId=umls:C0003873; sourceId=BeFree; sentence=We first investigated the association between the SNPs (rs2910164 G>C and rs3746444 T>C) in the pre-miRNA (hsa-mir-146a and hsa-mir-499) and RA in a Han Chinese population.; score=0.012973128; Year=2011; geneSymbol_dbSNP=MYH7B;MIR499A;MIR499B; CHROMOSOME=20; POS=34990448; REF=A; ALT=G |
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rs3746444 |
SNP |
PedAM |
snpId=rs3746444; pubmedId=22019503; geneId=406938; geneSymbol=MIR146A; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The aim of this study was to detect the association between 2 single nucleotide polymorphisms (SNPs), rs2910164 G>C and rs3746444 T>C, in pre-miRNA (hsa-mir-146a and hsa-mir-499) and the chronic inflammation in the Chinese Han population with rheumatoid arthritis (RA).; score=0.012973128; Year=2012; geneSymbol_dbSNP=MYH7B;MIR499A;MIR499B; CHROMOSOME=20; POS=34990448; REF=A; ALT=G |
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rs3746444 |
SNP |
PedAM |
snpId=rs3746444; pubmedId=22019503; geneId=574501; geneSymbol=MIR499A; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The results of this study provided the first evidence that the SNP rs3746444 in pre-miR-499 could affect the inflammatory reaction in patients with RA.; score=0.001357209; Year=2012; geneSymbol_dbSNP=MYH7B;MIR499A;MIR499B; CHROMOSOME=20; POS=34990448; REF=A; ALT=G |
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rs3746444 |
SNP |
PedAM |
snpId=rs3746444; pubmedId=21181275; geneId=574501; geneSymbol=MIR499A; diseaseId=umls:C0003873; sourceId=BeFree; sentence=We first investigated the association between the SNPs (rs2910164 G>C and rs3746444 T>C) in the pre-miRNA (hsa-mir-146a and hsa-mir-499) and RA in a Han Chinese population.; score=0.001357209; Year=2011; geneSymbol_dbSNP=MYH7B;MIR499A;MIR499B; CHROMOSOME=20; POS=34990448; REF=A; ALT=G |
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rs3761847 |
SNP |
PedAM |
snpId=rs3761847; pubmedId=20453842; geneId=7185; geneSymbol=TRAF1; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.; score=0.311201237; Year=2010; geneSymbol_dbSNP=TRAF1; CHROMOSOME=9; POS=120927961; REF=G; ALT=A |
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rs3761847 |
SNP |
PedAM |
snpId=rs3761847; pubmedId=19714643; geneId=26147; geneSymbol=PHF19; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Our results demonstrate that within and around TRAF1, excluding PHF19 and C5, SNPs highly correlated with rs7021206, but not those correlated with rs3761847, are associated with RA in both Asians and Caucasians and are possibly correlated with causative variations.; score=0.122638474; Year=2009; geneSymbol_dbSNP=TRAF1; CHROMOSOME=9; POS=120927961; REF=G; ALT=A |
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rs3761847 |
SNP |
PedAM |
snpId=rs3761847; pubmedId=19116907; geneId=7185; geneSymbol=TRAF1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The risk of death in RA is increased in TRAF1/C5 rs3761847 GG homozygotes and appears to be independent of RA activity and severity as well as comorbidities relevant to CVD.; score=0.311201237; Year=2009; geneSymbol_dbSNP=TRAF1; CHROMOSOME=9; POS=120927961; REF=G; ALT=A |
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rs3761847 |
SNP |
PedAM |
snpId=rs3761847; pubmedId=17804836; geneId=7185; geneSymbol=TRAF1; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.; score=0.311201237; Year=2007; geneSymbol_dbSNP=TRAF1; CHROMOSOME=9; POS=120927961; REF=G; ALT=A |
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rs3761847 |
SNP |
PedAM |
snpId=rs3761847; pubmedId=21492465; geneId=26191; geneSymbol=PTPN22; diseaseId=umls:C0003873; sourceId=BeFree; sentence=We genotyped SNPs rs3761847 and rs7021206 at the TRAF1/C5 locus and rs2476601 SNP in the PTPN22 gene in a Han Chinese cohort composed of 576 patients with RA and 689 controls.; score=0.524345611; Year=2011; geneSymbol_dbSNP=TRAF1; CHROMOSOME=9; POS=120927961; REF=G; ALT=A |
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rs3761847 |
SNP |
PedAM |
snpId=rs3761847; pubmedId=19445664; geneId=7185; geneSymbol=TRAF1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=No statistically significant association of TRAF1/C5 SNPs rs3761847 and rs10818488 with RA was detected.; score=0.311201237; Year=2009; geneSymbol_dbSNP=TRAF1; CHROMOSOME=9; POS=120927961; REF=G; ALT=A |
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rs3761847 |
SNP |
PedAM |
snpId=rs3761847; pubmedId=23125866; geneId=7185; geneSymbol=TRAF1; diseaseId=umls:C0003873; sourceId=BeFree; sentence=To assess the frequency of the RA-conferring susceptibility TRAF1 polymorphisms rs3761847 and rs2900180 in a cohort of PBC patients.; score=0.311201237; Year=2012; geneSymbol_dbSNP=TRAF1; CHROMOSOME=9; POS=120927961; REF=G; ALT=A |
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rs3763309 |
SNP |
PedAM |
snpId=rs3763309; pubmedId=24449572; geneId=56244; geneSymbol=BTNL2; diseaseId=umls:C0003873; sourceId=GWASCAT; sentence=Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study.; score=0.128001298; Year=2013; geneSymbol_dbSNP=BTNL2;LOC101929163; CHROMOSOME=6; POS=32408196; REF=C; ALT=A |
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rs3768777 |
SNP |
PedAM |
snpId=rs3768777; pubmedId=24375314; geneId=3685; geneSymbol=ITGAV; diseaseId=umls:C0003873; sourceId=BeFree; sentence=The rs3768777-G allele of ITGAV gene is associated with rheumatoid arthritis.; score=0.008815624; Year=2013; geneSymbol_dbSNP=ITGAV; CHROMOSOME=2; POS=186591394; REF=A; ALT=G |
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rs3781913 |
SNP |
PedAM |
snpId=rs3781913; pubmedId=23577190; geneId=5771; geneSymbol=PTPN2; diseaseId=umls:C0003873; sourceId=BeFree; sentence=Genetic factors regarded as putative risk factors were RA-susceptible polymorphisms identified by the Japanese GWAS meta-analysis, including HLA-DRB1 (shared epitope, SE), rs2240340 (PADI4), rs2230926 (TNFAIP3), rs3093024 (CCR6), rs11900673 (B3GNT2), rs2867461 (ANXA3), rs657075 (CSF2), rs12529514 (CD83), rs2233434 (NFKBIE), rs10821944 (ARID5B), rs3781913 (PDE2A-ARAP1), rs2841277 (PLD4) and rs2847297 (PTPN2).; score=0.248458305; Year=2013; geneSymbol_dbSNP=PDE2A;LOC105369379; CHROMOSOME=11; POS=72662452; REF=T; ALT=G |
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