rs758368355, TPO

N. diseases: 1
Disease: Familial dyshormonogenetic goiter ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial dyshormonogenetic goiter
CUI: C0342191
Disease: Familial dyshormonogenetic goiter
0.010 GeneticVariation BEFREE The detection of the novel c.670_672del and c.1186C>T alterations expand the mutation spectrum of TPO associated with thyroid dyshormonogenesis. 25564141 2015