Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607552
rs267607552
LMNA
A 0.700 CausalMutation CLINVAR Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy. 18585512

2008
dbSNP: rs267607552
rs267607552
LMNA
A 0.700 CausalMutation CLINVAR Long-term outcome and risk stratification in dilated cardiolaminopathies. 18926329

2008