Variant: rs56851164 

    present in Gene: LMNA
    present in Chromosome: 1
    Position on Chromosome: 156135940
    Alleles of this Variant: T/A

rs56851164 in LMNA gene and Cardiomyopathy, Hypertrophic, Familial PMID 16407522 2006 Primary prevention of sudden death in patients with lamin A/C gene mutations.

PMID 24503780 2014 The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.

PMID 16585054 2006 Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins.