|
rs727503499
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Development of a high resolution melting method for the detection of genetic variations in hypertrophic cardiomyopathy.
|
20800588 |
2010 |
|
rs727503503
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy.
|
20031618 |
2009 |
|
rs727503504
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy.
|
20031618 |
2009 |
|
rs397516153
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A de novo mutation of the beta cardiac myosin heavy chain gene in an infantile restrictive cardiomyopathy.
|
18380764 |
2008 |
|
rs727503260
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Pediatric restrictive cardiomyopathy associated with a mutation in beta-myosin heavy chain.
|
18076673 |
2008 |
|
rs727503503
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype.
|
17599605 |
2007 |
|
rs727503260
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy].
|
17125710 |
2006 |
|
rs727503260
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
|
12707239 |
2003 |
|
rs727503513
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy.
|
10525521 |
1999 |
|
rs1294950721
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1554401403
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs727503269
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs730880231
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs121918312
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The BAG3-Pro209Leu mutation is associated with early onset MFM and severe restrictive cardiomyopathy (RCM), often necessitating heart transplantation during childhood.
|
29338979 |
2018 |
|
rs104894724
|
|
|
0.020 |
GeneticVariation |
BEFREE |
These perturbed biophysical and biochemical myofilament properties are likely to significantly contribute to the diastolic cardiac pump dysfunction that is seen in patients suffering from a restrictive cardiomyopathy that is associated with the cTnI R145W mutation.
|
27557662 |
2016 |
|
rs121918312
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Genetic testing demonstrated heterozygous mutation Pro209Leu (c.626C > T) in exon 3 of BAG3 gene causing severe myopathy and neuropathy, often associated with restrictive cardiomyopathy.
|
26545904 |
2015 |
|
rs104894724
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Functional effects of a restrictive-cardiomyopathy-linked cardiac troponin I mutation (R145W) in transgenic mice.
|
19651143 |
2009 |
|
rs1114167361
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here, we report a new clinical phenotype of filaminopathy in four unrelated patients with early-onset restrictive cardiomyopathy (RCM) in combination with congenital myopathy due to FLNC mutations (NM_001458.4:c.3557C>T, p.A1186V, rs1114167361 in three probands and c.[3547G>C; 3548C>T], p.A1183L, rs1131692185 in one proband).
|
29858533 |
2018 |
|
rs1131692185
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Here, we report a new clinical phenotype of filaminopathy in four unrelated patients with early-onset restrictive cardiomyopathy (RCM) in combination with congenital myopathy due to FLNC mutations (NM_001458.4:c.3557C>T, p.A1186V, rs1114167361 in three probands and c.[3547G>C; 3548C>T], p.A1183L, rs1131692185 in one proband).
|
29858533 |
2018 |
|
rs34677717
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The BAG3-Pro209Leu mutation is associated with early onset MFM and severe restrictive cardiomyopathy (RCM), often necessitating heart transplantation during childhood.
|
29338979 |
2018 |
|
rs1114167341
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The novel αB-crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathy.
|
28493373 |
2017 |
|
rs1204336259
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The E143K (Glu → Lys) mutation in the myosin essential light chain has been associated with restrictive cardiomyopathy (RCM) in humans, but the mechanisms that underlie the development of defective cardiac function are unknown.
|
28371863 |
2017 |
|
rs141754300
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We describe a pediatric proband with fatal restrictive cardiomyopathy associated with septal hypertrophy and compound heterozygosity for TNNC1 mutations (NM_003280: p.A8V [c.C23T] and p.D145E [c.C435A]).
|
27604170 |
2016 |
|
rs200754249
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We describe a pediatric proband with fatal restrictive cardiomyopathy associated with septal hypertrophy and compound heterozygosity for TNNC1 mutations (NM_003280: p.A8V [c.C23T] and p.D145E [c.C435A]).
|
27604170 |
2016 |
|
rs267607124
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We describe a pediatric proband with fatal restrictive cardiomyopathy associated with septal hypertrophy and compound heterozygosity for TNNC1 mutations (NM_003280: p.A8V [c.C23T] and p.D145E [c.C435A]).
|
27604170 |
2016 |