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: rs3783938
rs3783938
Entrez Id: 7253;101928462
Gene Symbol: TSHR;LOC101928462
TSHR;LOC101928462
CUI: C0018213
Disease:
Graves Disease 		0.010 GeneticVariation BEFREE These data suggest that the polymorphisms of rs12101255 and rs3783938 are associated with GD and HT, respectively. 22673349 2012