Variant: rs397516089 

    present in Gene: MYH7
    present in Chromosome: 14
    Position on Chromosome: 23429807
    Alleles of this Variant: C/G;T

rs397516089 in MYH7 gene and Cardiomyopathy, Dilated PMID 27532257 2017 Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.

PMID 20031619 2009 Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.

PMID 22464770 2012 Genetic testing for dilated cardiomyopathy in clinical practice.

PMID 24691700 2015 A low prevalence of sarcomeric gene variants in a Chinese cohort with left ventricular non-compaction.

rs397516089 in MYH7 gene and Cardiomyopathy, Hypertrophic, Familial PMID 24503780 2014 The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.

PMID 20530761 2010 The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy.

PMID 20031619 2009 Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.

PMID 24691700 2015 A low prevalence of sarcomeric gene variants in a Chinese cohort with left ventricular non-compaction.

rs397516089 in MYH7 gene and Left ventricular noncompaction PMID 24691700 2015 A low prevalence of sarcomeric gene variants in a Chinese cohort with left ventricular non-compaction.

PMID 22464770 2012 Genetic testing for dilated cardiomyopathy in clinical practice.

PMID 20031619 2009 Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.