|
rs116855232
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In this report, we first provide detailed clinical and laboratory characteristics of AZA-induced leukopenia in a patient with SS with a mutant NUDT15 R139C genotype (TT allele) and normal TPMT activity.
|
29702976 |
2018 |
|
rs61756766
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A BAFF receptor His159Tyr mutation in Sjögren's syndrome-related lymphoproliferation.
|
26097183 |
2015 |
|
rs387907272
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Although the absence of the MyD88 L265P somatic mutation in our SS cohort does not exclude a common germline susceptibility gene in SS, it might suggest a distinct operating pathogenetic mechanism in SS-related lymphoma compared with WM and other hematological malignancies.
|
24153350 |
2014 |
|
rs774359492
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Thirteen articles with 21 comparison studies (16 on FAS -670 A/G and 5 on -1,377 G/A polymorphisms) including systemic lupus erythematosus (SLE), four systemic sclerosis, four Sjogren's syndrome, three rheumatoid arthritis (RA), one juvenile idiopathic arthritis, and one spondyloarthropathy were available for the meta-analysis.
|
23053964 |
2012 |
|
rs1143634
|
|
|
0.010 |
GeneticVariation |
BEFREE |
It is suggested that rs1143634 of IL1B and rs8192284 of IL6R act as susceptibility variations in Korean non-Sjogren dry eye patients.
|
22128229 |
2011 |
|
rs8192284
|
|
|
0.010 |
GeneticVariation |
BEFREE |
It is suggested that rs1143634 of IL1B and rs8192284 of IL6R act as susceptibility variations in Korean non-Sjogren dry eye patients.
|
22128229 |
2011 |
|
rs1004819
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods.
|
19522770 |
2009 |
|
rs10489629
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods.
|
19522770 |
2009 |
|
rs10889677
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods.
|
19522770 |
2009 |
|
rs11209026
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods.
|
19522770 |
2009 |
|
rs11209032
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods.
|
19522770 |
2009 |
|
rs11805303
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods.
|
19522770 |
2009 |
|
rs2201841
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods.
|
19522770 |
2009 |
|
rs7517847
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods.
|
19522770 |
2009 |
|
rs7530511
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods.
|
19522770 |
2009 |
|
rs1085308048
|
|
|
0.010 |
GeneticVariation |
BEFREE |
This report describes a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndrome.
|
10193515 |
1998 |
|
rs2230926
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Increased prevalence of the rs2230926 mutant variant was detected in both SS-lymphoma and SS-nonlymphoma subgroups compared to HC (8.8% vs. 7.6% vs. 3.6%, <i>p</i> values: 0.04 and 0.03, respectively) in association with higher IgM, LDH serum levels, and PB <i>Bcl-XL</i> transcripts but lower leucocyte and neutrophil counts.
|
30662920 |
2018 |
|
rs10774671
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The SS risk allele of rs10774671 has been shown by others to be associated with reduced OAS1 enzymatic activity and ability to clear viral infections, as well as reduced responsiveness to IFN treatment.
|
28640813 |
2017 |
|
rs10774671
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Our data demonstrated that the functional variant, rs10774671, is associated with HBV infection and anti-SSA antibody-positive SS.
|
29242559 |
2017 |
|
rs2230926
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Genotyping of the most common coding polymorphism, rs2230926, in the MADGC collection and additional control individuals revealed a significant association with Sjögren's syndrome (OR=3.38, P=0.038), Crohn's disease (OR=2.25, P=0.041), psoriasis (OR=0.037, P=0.036) and RA (OR=1.9, P=0.025).
|
21326317 |
2011 |
|
rs11048434
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry.
|
28076899 |
2017 |
|
rs11889341
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry.
|
28076899 |
2017 |
|
rs17074492
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry.
|
28076899 |
2017 |
|
rs1957173
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry.
|
28076899 |
2017 |
|
rs3823536
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry.
|
28076899 |
2017 |