rs1060502214
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1060502215
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Specific phosphorylation of Ser458 of A-type lamins in LMNA-associated myopathy patients.
|
20980393 |
2010 |
rs1553261891
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1553265606
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Long-term outcome and risk stratification in dilated cardiolaminopathies.
|
18926329 |
2008 |
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 |
rs1553265733
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1553265924
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Long-term outcome and risk stratification in dilated cardiolaminopathies.
|
18926329 |
2008 |
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 |
rs267607632
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs397517912
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
|
24503780 |
2014 |
rs397517912
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated Cardiomyopathy.
|
29367541 |
2017 |
rs397517912
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation.
|
29095976 |
2018 |
rs56793579
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs56984562
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.
|
23183350 |
2013 |
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 |
rs56984562
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
rs56984562
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.
|
18646565 |
2007 |
rs56984562
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy.
|
16218190 |
2005 |
rs56984562
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Laminopathies in Russian families.
|
18564364 |
2008 |
rs56984562
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes.
|
14684700 |
2003 |
rs58436778
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs869125101
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Long-term outcome and risk stratification in dilated cardiolaminopathies.
|
18926329 |
2008 |
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 |
rs879253934
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs886043109
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Specific phosphorylation of Ser458 of A-type lamins in LMNA-associated myopathy patients.
|
20980393 |
2010 |