Variant: rs730880800 

    present in Gene: MYH7;MHRT;MIR208B
    present in Chromosome: 14
    Position on Chromosome: 23417556
    Alleles of this Variant: G/A

rs730880800 in MYH7;MHRT;MIR208B gene and Cardiomyopathy, Hypertrophic, Familial PMID 24119082 2013 Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.

PMID 21750094 2011 Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.

PMID 21310275 2011 Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.

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