Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61661343
rs61661343
LMNA
0.020 GeneticVariation BEFREE Deleterious assembly of the lamin A/C mutant p.S143P causes ER stress in familial dilated cardiomyopathy. 27235420

2016
dbSNP: rs61661343
rs61661343
LMNA
0.020 GeneticVariation BEFREE A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy. 15140538

2004