rs121434591, MATR3

N. diseases: 5
Disease: Hoarseness ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hoarseness
CUI: C0019825
Disease: Hoarseness
0.010 GeneticVariation BEFREE The p.S85C MATR3 variant was previously associated to a different phenotype, namely a distal myopathy associated with dysphagia and dysphonia. 28029397 2017