rs2076739, TG

N. diseases: 5
Disease: Dwarfism ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dwarfism
CUI: C0013336
Disease: Dwarfism
0.010 GeneticVariation BEFREE We have studied UPR development in two similar ERSDs, human congenital goiter caused by the C1264R and C1996S mutations in the thyroglobulin (Tg) gene and non-goitrous congenital hypothyroidism in rdw dwarf rats determined by the G2320R Tg mutation. 15171721 2004