CEP128, centrosomal protein 128, 145508

N. diseases: 14; N. variants: 13
Disease: Graves Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2239610
rs2239610
Entrez Id: 7253;145508
Gene Symbol: TSHR;CEP128
TSHR;CEP128
CUI: C0018213
Disease:
Graves Disease 		0.010 GeneticVariation BEFREE In addition, the TSHR rs2239610 SNP is related to the severity of Graves' disease. 19438904 2010