Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
BEFREE |
Genetic polymorphism (rs1800693) of TNFRSF1A (type 1 tumour necrosis factor receptor) encodes a potentially anti-inflammatory soluble truncated form of the p55 receptor, which is associated with predisposition to multiple sclerosis but protection against ankylosing spondylitis (AS).
|
29535371 |
2019 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
BEFREE |
In conclusion, our results provide support for a sex- and HLA-DRB1*15:01-independent association of TNFRSF1A rs1800</span>693 SNP with MS susceptibility, but not with age at disease onset, severity or rate of disability accumulation.
|
30009568 |
2018 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
BEFREE |
The MS disease aetiology is unknown, though a polymorphism of the TNFRSF1A gene, rs1800693, is known to confer an increased risk for MS.
|
29034884 |
2017 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
GWASCAT |
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation.
|
27386562 |
2016 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
BEFREE |
The TNF-α inverse association with relapse was only present among persons carrying the wild-type of the functional SNP rs1800693 in TNFRSF1A that has been previously associated with MS risk.
|
24790215 |
2015 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
BEFREE |
The MS rs1800693(G) susceptibility allele affects the magnitude of monocyte responses to TNF-α stimulation, and the TNF pathway may be one network in which the effect of multiple MS genes becomes integrated.
|
24174586 |
2013 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
GWASCAT |
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
|
24076602 |
2013 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
BEFREE |
TNFRSF1A polymorphisms rs1800693 and rs4149584 in patients with multiple sclerosis.
|
23624563 |
2013 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
BEFREE |
This indicates that the clinical experience with these drugs parallels the disease association of rs1800693, and that the MS-associated TNFR1 variant mimics the effect of TNF-blocking drugs.
|
22801493 |
2012 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
GWASDB |
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
|
21833088 |
2011 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
GWASCAT |
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
|
21833088 |
2011 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
BEFREE |
In the recently published meta-analysis of multiple sclerosis genome-wide association studies De Jager et al. identified three single nucleotide polymorphisms associated to MS: rs17824933 (CD6), rs1800693 (TNFRSF1A) and rs17445836 (61.5 kb from IRF8).
|
21552549 |
2011 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
GWASDB |
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.
|
19525953 |
2009 |
Multiple Sclerosis
|
|
0.880 |
GeneticVariation
|
GWASCAT |
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.
|
19525953 |
2009 |
Primary biliary cirrhosis
|
|
0.800 |
GeneticVariation
|
GWASCAT |
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways.
|
26394269 |
2015 |
Primary biliary cirrhosis
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.
|
22961000 |
2012 |
Primary biliary cirrhosis
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.
|
22961000 |
2012 |
Primary biliary cirrhosis
|
|
0.800 |
GeneticVariation
|
GWASDB |
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.
|
22961000 |
2012 |
Primary biliary cirrhosis
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.
|
21399635 |
2011 |
Primary biliary cirrhosis
|
|
0.800 |
GeneticVariation
|
GWASDB |
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.
|
21399635 |
2011 |
Biliary cirrhosis
|
|
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.
|
21399635 |
2011 |
Neuromyelitis Optica
|
|
0.020 |
GeneticVariation
|
BEFREE |
Among the 35 SNPs, only one, rs1800693 in the TNFRSF1A locus, was nominally associated with NMO (P = 0.045, OR = 1.550, 95% CI = 1.007-2.384).
|
24927785 |
2014 |
Neuromyelitis Optica
|
|
0.020 |
GeneticVariation
|
BEFREE |
Logistic analyses revealed that one SNP in CD6 (rs12288280, P = 0.04) and three SNPs in TNFRSF1A (rs767455, rs4149577 and rs1800693, P = 0.01-0.03) were associated with NMO.
|
22994200 |
2013 |
Ankylosing spondylitis
|
|
0.010 |
GeneticVariation
|
BEFREE |
Genetic polymorphism (rs1800693) of TNFRSF1A (type 1 tumour necrosis factor receptor) encodes a potentially anti-inflammatory soluble truncated form of the p55 receptor, which is associated with predisposition to multiple sclerosis but protection against ankylosing spondylitis (AS).
|
29535371 |
2019 |
Celiac Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
One TNFRSF1A variant was identified (c.625+10A>G, rs1800693), but not associated with CD.
|
25915602 |
2015 |