MYL4, myosin light chain 4, 4635

N. diseases: 26; N. variants: 5
Disease: familial atrial fibrillation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3468561
Disease: familial atrial fibrillation
familial atrial fibrillation 		0.100 CausalMutation phenotype CLINVAR A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation. 27066836 2016