rs28933408, THRB

N. diseases: 3
Disease: Myotonic Dystrophy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myotonic Dystrophy
CUI: C0027126
Disease: Myotonic Dystrophy
0.010 GeneticVariation BEFREE Two Mutations in Thyroid Hormone Receptor Beta Gene (P453A and C36Y) in a Family with Resistance to Thyroid Hormone with Comorbid Myotonic Dystrophy. 30672388 2019