rs60682848, LMNA

N. diseases: 11
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myopathy
CUI: C0026848
Disease: Myopathy
0.010 GeneticVariation BEFREE Lmna R225X mutant mice hold the potential for serving as in vivo models to explore the mechanism and therapeutic methods for AV block or myopathy associated with the aging process. 31668660 2020