TG, thyroglobulin, 7038

N. diseases: 240; N. variants: 43
Disease: Graves Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2294025
rs2294025
Entrez Id: 7038
Gene Symbol: TG
TG
CUI: C0018213
Disease:
Graves Disease 		0.810 GeneticVariation BEFREE The fine mapping study of thyroglobulin identified two independent SNPs (rs2294025 and rs7005834) for GD susceptibility. 31700870 2019
dbSNP: rs2294025
rs2294025
Entrez Id: 7038
Gene Symbol: TG
TG
CUI: C0018213
Disease:
Graves Disease 		T 0.810 GeneticVariation GWASCAT Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. 23612905 2013
dbSNP: rs2294025
rs2294025
Entrez Id: 7038
Gene Symbol: TG
TG
CUI: C0018213
Disease:
Graves Disease 		T 0.810 GeneticVariation GWASDB Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. 23612905 2013