rs367761724

This variant is located in the MYL3 gene.

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ClinVar annotation

Likely Benign★★★☆
6 submitters3 publications

not specified; Cardiomyopathy; Hypertrophic cardiomyopathy; Cardiovascular phenotype

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About MYL3

MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]

View all MYL3 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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