Variant: rs878853220 

    present in Gene: LMNA
    present in Chromosome: 1
    Position on Chromosome: 156130818
    Alleles of this Variant: T/G

rs878853220 in LMNA gene and Abnormality of the calf musculature PMID 27717888 2016 New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.

rs878853220 in LMNA gene and Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) PMID 27717888 2016 New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.

rs878853220 in LMNA gene and Bradyarrhythmia (disorder) PMID 27717888 2016 New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.

rs878853220 in LMNA gene and Lumbar hyperlordosis PMID 27717888 2016 New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.

rs878853220 in LMNA gene and Premature ventricular contractions PMID 27717888 2016 New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.

rs878853220 in LMNA gene and Second degree atrioventricular block PMID 27717888 2016 New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.