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: rs179249
rs179249
Entrez Id: 7253
Gene Symbol: TSHR
TSHR
CUI: C0018213
Disease:
Graves Disease 		0.700 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011