Variant: rs267607581 

    present in Gene: LMNA
    present in Chromosome: 1
    Position on Chromosome: 156137651
    Alleles of this Variant: C/G

rs267607581 in LMNA gene and Cardiomyopathy, Dilated PMID 18714801 2008 A novel mutation in a large French-Canadian family with LGMD1B.

PMID 28679633 2017 Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.

PMID 25525159 2015 RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.

PMID 8621584 1996 An alternative splicing product of the lamin A/C gene lacks exon 10.

rs267607581 in LMNA gene and Neuromuscular Diseases PMID 25525159 2015 RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.

PMID 28679633 2017 Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing.

PMID 8621584 1996 An alternative splicing product of the lamin A/C gene lacks exon 10.

PMID 18714801 2008 A novel mutation in a large French-Canadian family with LGMD1B.