rs59270054, LMNA

N. diseases: 6
Disease: Cardiomyopathies ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
0.010 GeneticVariation BEFREE Mutation Glu82Lys in lamin A/C gene is associated with cardiomyopathy and conduction defect. 16630578 2006