|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.
|
28771489 |
2017 |
|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Burden of Recurrent and Ancestral Mutations in Families With Hypertrophic Cardiomyopathy.
|
28615295 |
2017 |
|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
|
27532257 |
2017 |
|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications.
|
28408708 |
2017 |
|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Detection of mutations in symptomatic patients with hypertrophic cardiomyopathy in Taiwan.
|
25086479 |
2015 |
|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noise.
|
24510615 |
2014 |
|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy.
|
23711808 |
2013 |
|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy.
|
24093860 |
2013 |
|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond.
|
20075948 |
2010 |
|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy.
|
12974739 |
2003 |
|
rs727503278
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Molecular etiology of idiopathic cardiomyopathy in Asian populations.
|
11433818 |
2001 |