|
rs231775
|
|
|
0.030 |
GeneticVariation |
BEFREE |
49A/G and CT60 polymorphisms of the cytotoxic T-lymphocyte-associated antigen 4 gene associated with autoimmune thyroid disease.
|
19559744 |
2009 |
|
rs231775
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Association of the CTLA-4 gene 49 A/G polymorphism with type 1 diabetes and autoimmune thyroid disease in Japanese children.
|
12610047 |
2003 |
|
rs231775
|
|
|
0.030 |
GeneticVariation |
BEFREE |
CTLA-4 and autoimmune thyroid disease: lack of influence of the A49G signal peptide polymorphism on functional recombinant human CTLA-4.
|
12202150 |
2002 |
|
rs2476601
|
|
|
0.020 |
GeneticVariation |
BEFREE |
No association was found between C1858T polymorphism and diabetes-related autoimmunity (p = 0.173) or thyroid autoimmune disease (p = 0.321), respectively.
|
20438787 |
2010 |
|
rs2476601
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The R620W polymorphism of the PTPN22 gene is not a major risk allele for SLE susceptibility in our sample of Caucasian individuals from northern America, the UK, or Finland, but it appears to be a risk factor for the concurrent autoimmune diseases of autoimmune thyroid disease and SLE.
|
16052563 |
2005 |
|
rs2276886
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Recently, the single nucleotide polymorphism (SNP) rs2276886 associated with the <i>CXCL9</i> gene was identified as associated with autoimmune thyroid disease susceptibility in Japanese populations.
|
31750736 |
2019 |
|
rs7574865
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The Association Between <i>STAT4</i> rs7574865 Polymorphism and the Susceptibility of Autoimmune Thyroid Disease: A Meta-Analysis.
|
30666271 |
2018 |
|
rs3792876
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Association of single nucleotide polymorphism rs3792876 in SLC22A4 gene with autoimmune thyroid disease in a Chinese Han population.
|
26329403 |
2015 |
|
rs10930046
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study we analyzed IFIH1 rs6432714 and rs10930046 SNPs in T1D patients stratified for the presence of celiac disease and autoimmune thyroid disease.
|
23246693 |
2013 |
|
rs2291282
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We genotyped six single-nucleotide polymorphisms (SNPs) rs1053005, rs2293152, rs744166, rs17593222, rs2291281, and rs2291282 of STAT3 gene in 667 patients with autoimmune thyroid disease (417 Graves' disease (GD) and 250 Hashimoto's thyroiditis (HT)) and 301 healthy controls.
|
24081513 |
2013 |
|
rs6432714
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In our study we analyzed IFIH1 rs6432714 and rs10930046 SNPs in T1D patients stratified for the presence of celiac disease and autoimmune thyroid disease.
|
23246693 |
2013 |
|
rs2072895
|
|
|
0.010 |
GeneticVariation |
BEFREE |
One of them was as follows: rs2072895 (non_synonymous_coding & splice-site) and rs2735059 (non_synonymous_coding) → HLA-F → type I diabetes mellitus, antigen processing and presentation, and autoimmune thyroid disease.
|
22201026 |
2012 |
|
rs2735059
|
|
|
0.010 |
GeneticVariation |
BEFREE |
One of them was as follows: rs2072895 (non_synonymous_coding & splice-site) and rs2735059 (non_synonymous_coding) → HLA-F → type I diabetes mellitus, antigen processing and presentation, and autoimmune thyroid disease.
|
22201026 |
2012 |
|
rs1167204443
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Association of the CTLA-4 gene 49 A/G polymorphism with type 1 diabetes and autoimmune thyroid disease in Japanese children.
|
12610047 |
2003 |
|
rs17879469
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Association of the CTLA-4 gene 49 A/G polymorphism with type 1 diabetes and autoimmune thyroid disease in Japanese children.
|
12610047 |
2003 |
|
rs1190356035
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Frequencies of autoimmunity characteristics (ICA or GAD-Ab positiveness and combination of autoimmune thyroid disease) were decreased in the R456H-positive patients compared to the R456H-negative patients.
|
10679252 |
2000 |
|
rs1801208
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Frequencies of autoimmunity characteristics (ICA or GAD-Ab positiveness and combination of autoimmune thyroid disease) were decreased in the R456H-positive patients compared to the R456H-negative patients.
|
10679252 |
2000 |
|
rs751054919
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Three of the TSH receptor mutants, deletions of residues 295-306 and 387-395 and the point mutation of cysteine 301 to serine, are shown to be particularly useful in these assays and may be useful to clarify the pathogenetic role and clinical significance of stimulating TSHRAbs in patients with autoimmune thyroid disease who also have blocking TSHRAbs.
|
8100829 |
1993 |