rs60682848, LMNA

N. diseases: 11
Disease: Familial dilated cardiomyopathy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial dilated cardiomyopathy
CUI: C0340427
Disease: Familial dilated cardiomyopathy
0.010 GeneticVariation BEFREE We identified an autosomal dominant non‐sense mutation (R225X) in exon 4 of the lamin A/C (LMNA) gene in a Chinese family spanning 3 generations with familial dilated cardiomyopathy (DCM). 23362510 2012