rs61195471, LMNA

N. diseases: 6
Disease: Heart failure ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Heart failure
CUI: C0018801
Disease: Heart failure
0.010 GeneticVariation BEFREE In family A a missense mutation (nucleotide G607A, amino acid E203K) was identified in 14 adult subjects; disease was manifest as progressive conduction disease in the fourth and fifth decades.Death was caused by heart failure. 11561226 2001