rs2476601
|
|
|
0.740 |
GeneticVariation |
BEFREE |
This meta-analysis shows a significant association between PTPN22 R620W polymorphism and MG risk.
|
26318187 |
2015 |
rs2476601
|
|
|
0.740 |
GeneticVariation |
BEFREE |
DNA samples from 416 patients with clinically diagnosed generalized MG (231 with Abs to acetylcholine receptor, AChR-MG), 53 with Abs to muscle-specific kinase (MuSK-MG), 55 patients with no detectable Abs (SN-MG), 77 patients with thymoma (TAMG) and 293 healthy controls (HC) were genotyped for the SNP (PTPN22 R620W, C1858T, rs2476601).
|
25119822 |
2014 |
rs2476601
|
|
A |
0.740 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
rs2476601
|
|
|
0.740 |
GeneticVariation |
BEFREE |
We conclude that the common autoimmune polymorphism PTPN22 1858C/T may account for disease susceptibility in a subset of nonthymoma MG patients with anti-titin antibodies present.
|
19406179 |
2009 |
rs2476601
|
|
|
0.740 |
GeneticVariation |
BEFREE |
PTPN22 R620W promotes production of anti-AChR autoantibodies and IL-2 in myasthenia gravis.
|
18533277 |
2008 |
rs111945767
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations.
|
26562150 |
2016 |
rs12653117
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations.
|
26562150 |
2016 |
rs150881176
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations.
|
26562150 |
2016 |
rs2071591
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations.
|
26562150 |
2016 |
rs4574025
|
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations.
|
26562150 |
2016 |
rs6998967
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations.
|
26562150 |
2016 |
rs9963862
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations.
|
26562150 |
2016 |
rs231770
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study of myasthenia gravis.
|
25643325 |
2015 |
rs4263037
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study of myasthenia gravis.
|
25643325 |
2015 |
rs9270986
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
A genome-wide association study of myasthenia gravis.
|
25643325 |
2015 |
rs11229
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
rs1235162
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
rs1265159
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
rs1270942
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
rs1422673
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
rs1634718
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
rs1794282
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
rs1980493
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
rs204990
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |
rs2187668
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
|
23055271 |
2012 |