×
Entrez Id:
26191
Gene Symbol:
PTPN22
PTPN22
0.500
GeneticVariation
disease
GWASDB
Seven newly identified loci for autoimmune thyroid disease.
22922229
2012
×
Entrez Id:
7253
Gene Symbol:
TSHR
TSHR
0.500
GeneticVariation
disease
GWASDB
Seven newly identified loci for autoimmune thyroid disease.
22922229
2012
×
Entrez Id:
7253
Gene Symbol:
TSHR
TSHR
0.500
GeneticVariation
disease
GWASDB
Moreover, we identified strong associations of TSHR and major histocompatibility complex class II variants with persistently TRAb-positive Graves' disease .
21841780
2011
×
Entrez Id:
115352
Gene Symbol:
FCRL3
FCRL3
0.480
GeneticVariation
disease
GWASDB
A genome-wide association study identifies two new risk loci for Graves' disease.
21841780
2011
×
Entrez Id:
7124
Gene Symbol:
TNF
TNF
0.200
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011
×
Entrez Id:
3105
Gene Symbol:
HLA-A
HLA-A
0.200
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011
×
Entrez Id:
7038
Gene Symbol:
TG
TG
0.200
GeneticVariation
disease
GWASDB
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
23612905
2013
×
Entrez Id:
3106
Gene Symbol:
HLA-B
HLA-B
0.190
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011
×
Entrez Id:
114904
Gene Symbol:
C1QTNF6
C1QTNF6
0.120
GeneticVariation
disease
GWASDB
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
23612905
2013
×
Entrez Id:
5880
Gene Symbol:
RAC2
RAC2
0.120
GeneticVariation
disease
GWASDB
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
23612905
2013
×
Entrez Id:
6891
Gene Symbol:
TAP2
TAP2
0.120
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011
×
Entrez Id:
145508
Gene Symbol:
CEP128
CEP128
0.110
GeneticVariation
disease
GWASDB
A genome-wide association study identifies two new risk loci for Graves' disease.
21841780
2011
×
Entrez Id:
3710
Gene Symbol:
ITPR3
ITPR3
0.110
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011
×
Entrez Id:
115350
Gene Symbol:
FCRL1
FCRL1
0.110
GeneticVariation
disease
GWASDB
A genome-wide association study identifies two new risk loci for Graves' disease.
21841780
2011
×
Entrez Id:
28
Gene Symbol:
ABO
ABO
0.110
GeneticVariation
disease
GWASDB
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
23612905
2013
×
Entrez Id:
114836
Gene Symbol:
SLAMF6
SLAMF6
0.110
GeneticVariation
disease
GWASDB
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
23612905
2013
PRICKLE1
0.100
GeneticVariation
disease
GWASDB
Seven newly identified loci for autoimmune thyroid disease.
22922229
2012
×
Entrez Id:
1041
Gene Symbol:
CDSN
CDSN
0.100
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011
PSORS1C1
0.100
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011
×
Entrez Id:
6503
Gene Symbol:
SLA
SLA
0.100
GeneticVariation
disease
GWASDB
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
23612905
2013
×
Entrez Id:
100431177
Gene Symbol:
BHLHB9P1
BHLHB9P1
0.100
GeneticVariation
disease
GWASDB
A genome-wide association study identifies two new risk loci for Graves' disease.
21841780
2011
×
Entrez Id:
54535
Gene Symbol:
CCHCR1
CCHCR1
0.100
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011
×
Entrez Id:
100507679
Gene Symbol:
MUC22
MUC22
0.100
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011
ZNRD1ASP
0.100
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011
ATP6V1G2-DDX39B
0.100
GeneticVariation
disease
GWASDB
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
21900946
2011