ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.3645G>A (p.Val1215=)

dbSNP: rs936551123
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002117754 SCV002401967 likely benign Hypertrophic cardiomyopathy 14 2022-04-06 criteria provided, single submitter clinical testing

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