Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060502214
rs1060502214
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060502215
rs1060502215
T 0.700 GeneticVariation CLINVAR Specific phosphorylation of Ser458 of A-type lamins in LMNA-associated myopathy patients. 20980393

2010

dbSNP: rs1553261891
rs1553261891
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553265606
rs1553265606
A 0.700 GeneticVariation CLINVAR Long-term outcome and risk stratification in dilated cardiolaminopathies. 18926329

2008

dbSNP: rs1553265606
rs1553265606
A 0.700 GeneticVariation CLINVAR Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy. 18585512

2008

dbSNP: rs1553265733
rs1553265733
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553265924
rs1553265924
G 0.700 GeneticVariation CLINVAR Long-term outcome and risk stratification in dilated cardiolaminopathies. 18926329

2008

dbSNP: rs1553265924
rs1553265924
G 0.700 GeneticVariation CLINVAR Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy. 18585512

2008

dbSNP: rs267607632
rs267607632
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397517912
rs397517912
A 0.700 GeneticVariation CLINVAR The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing. 24503780

2014

dbSNP: rs397517912
rs397517912
A 0.700 GeneticVariation CLINVAR Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated Cardiomyopathy. 29367541

2017

dbSNP: rs397517912
rs397517912
A 0.700 GeneticVariation CLINVAR Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation. 29095976

2018

dbSNP: rs56793579
rs56793579
T 0.700 GeneticVariation CLINVAR

dbSNP: rs56984562
rs56984562
A 0.700 GeneticVariation CLINVAR Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers. 23183350

2013

dbSNP: rs56984562
rs56984562
A 0.700 GeneticVariation CLINVAR In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients. 16061563

2005

dbSNP: rs56984562
rs56984562
A 0.700 GeneticVariation CLINVAR Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257

2017

dbSNP: rs56984562
rs56984562
A 0.700 GeneticVariation CLINVAR Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan. 18646565

2007

dbSNP: rs56984562
rs56984562
A 0.700 GeneticVariation CLINVAR Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy. 16218190

2005

dbSNP: rs56984562
rs56984562
A 0.700 GeneticVariation CLINVAR Laminopathies in Russian families. 18564364

2008

dbSNP: rs56984562
rs56984562
A 0.700 GeneticVariation CLINVAR Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes. 14684700

2003

dbSNP: rs58436778
rs58436778
G 0.700 GeneticVariation CLINVAR

dbSNP: rs869125101
rs869125101
A 0.700 GeneticVariation CLINVAR Long-term outcome and risk stratification in dilated cardiolaminopathies. 18926329

2008

dbSNP: rs869125101
rs869125101
A 0.700 GeneticVariation CLINVAR Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy. 18585512

2008

dbSNP: rs879253934
rs879253934
C 0.700 GeneticVariation CLINVAR

dbSNP: rs886043109
rs886043109
A 0.700 GeneticVariation CLINVAR Specific phosphorylation of Ser458 of A-type lamins in LMNA-associated myopathy patients. 20980393

2010