Variant: rs1057515421 

    present in Gene: LMNA
    present in Chromosome: 1
    Position on Chromosome: 156136284
    Alleles of this Variant: C/T

rs1057515421 in LMNA gene and Cardiomyopathy, Familial Idiopathic PMID 10580070 1999 Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.

PMID 27760138 2016 Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.