Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26191
Gene Symbol: PTPN22
PTPN22
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.500 GeneticVariation GWASDB Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
Entrez Id: 7253
Gene Symbol: TSHR
TSHR
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.500 GeneticVariation GWASDB Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
Entrez Id: 7253
Gene Symbol: TSHR
TSHR
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.500 GeneticVariation 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
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.480 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780

2011
Entrez Id: 7038
Gene Symbol: TG
TG
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.200 GeneticVariation GWASDB Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. 23612905

2013
Entrez Id: 7124
Gene Symbol: TNF
TNF
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.200 GeneticVariation 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
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.200 GeneticVariation GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946

2011
Entrez Id: 3106
Gene Symbol: HLA-B
HLA-B
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.190 GeneticVariation 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
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.120 GeneticVariation 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
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.120 GeneticVariation 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
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.120 GeneticVariation GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946

2011
Entrez Id: 28
Gene Symbol: ABO
ABO
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.110 GeneticVariation 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
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.110 GeneticVariation GWASDB Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. 23612905

2013
Entrez Id: 145508
Gene Symbol: CEP128
CEP128
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.110 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780

2011
Entrez Id: 3710
Gene Symbol: ITPR3
ITPR3
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.110 GeneticVariation 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
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.110 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780

2011
Entrez Id: 6503
Gene Symbol: SLA
SLA
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASDB Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. 23612905

2013
Entrez Id: 144165
Gene Symbol: PRICKLE1
PRICKLE1
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASDB Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
Entrez Id: 4026
Gene Symbol: LPP
LPP
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASDB Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
Entrez Id: 11116
Gene Symbol: FGFR1OP
FGFR1OP
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASDB Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
Entrez Id: 79258
Gene Symbol: MMEL1
MMEL1
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASDB Seven newly identified loci for autoimmune thyroid disease. 22922229

2012
Entrez Id: 1041
Gene Symbol: CDSN
CDSN
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946

2011
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946

2011
Entrez Id: 100431177
Gene Symbol: BHLHB9P1
BHLHB9P1
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780

2011
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.100 GeneticVariation GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946

2011