ClinVar Miner

List of variants reported as uncertain significance for Hypertrophic cardiomyopathy 14 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.1328G>A (p.Arg443His)	rs202096001	0.00007
NM_002471.4(MYH6):c.343T>C (p.Tyr115His)	rs777804028	0.00001

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