rs104894655
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.
|
10655062 |
2000 |
rs1064793814
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Truncations of titin causing dilated cardiomyopathy.
|
22335739 |
2012 |
rs1114167453
|
|
Cardiomyopathy, Dilated
|
C |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs111569862
|
|
Cardiomyopathy, Dilated
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers.
|
27884249 |
2016 |
rs111569862
|
|
Cardiomyopathy, Dilated
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
A novel mutation in a large French-Canadian family with LGMD1B.
|
18714801 |
2008 |
rs112188483
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs112240298
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs114638163
|
|
Cardiomyopathy, Dilated
|
A |
0.700 |
CausalMutation
|
CLINVAR |
MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.
|
27799064 |
2016 |
rs121912997
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs121913642
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Elevated rates of force development and MgATP binding in F764L and S532P myosin mutations causing dilated cardiomyopathy.
|
23313350 |
2013 |
rs121913642
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathy.
|
22949430 |
2012 |
rs121913642
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse alpha-cardiac myosin in the laser trap assay.
|
17351073 |
2007 |
rs121913642
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.
|
16983074 |
2006 |
rs121913642
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
|
11106718 |
2000 |
rs121913642
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Human growth hormone stimulates somatomedin C/insulin-like growth factor I production by the human lymphoid cell line, IM-9.
|
2753225 |
1989 |
rs121913647
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs137853197
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy.
|
19881492 |
2009 |
rs140614802
|
|
Cardiomyopathy, Dilated
|
A |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs140743001
|
|
Cardiomyopathy, Dilated
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
|
24503780 |
2014 |
rs140743001
|
|
Cardiomyopathy, Dilated
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Truncations of titin causing dilated cardiomyopathy.
|
22335739 |
2012 |
rs1408345511
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs143139258
|
|
Cardiomyopathy, Dilated
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs148894066
|
|
Cardiomyopathy, Dilated
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
|
|
|
rs150974575
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
Compound heterozygosity of predicted loss-of-function DES variants in a family with recessive desminopathy.
|
23815709 |
2013 |
rs150974575
|
|
Cardiomyopathy, Dilated
|
T |
0.700 |
GeneticVariation
|
CLINVAR |
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.
|
22153487 |
2012 |