TSHR, thyroid stimulating hormone receptor, 7253

N. diseases: 250; N. variants: 77
Disease: Graves Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8022600
rs8022600
Entrez Id: 7253;145508
Gene Symbol: TSHR;CEP128
TSHR;CEP128
CUI: C0018213
Disease:
Graves Disease 		0.700 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011