ClinVar Miner

List of variants reported as not provided for Hypertrophic cardiomyopathy 1; Left ventricular noncompaction 1; Myopathy, myosin storage, autosomal recessive; Myosin storage myopathy; Congenital myopathy with fiber type disproportion; Dilated cardiomyopathy 1S; MYH7-related skeletal myopathy; MYH7-related disorder

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_000257.4(MYH7):c.3711G>C (p.Gln1237His) rs1361182615

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