rs886037778, MYL4

N. diseases: 2
Disease: familial atrial fibrillation ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
familial atrial fibrillation
CUI: C3468561
Disease: familial atrial fibrillation
0.700 CausalMutation CLINVAR A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation. 27066836 2016