ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.5652C>A (p.Ala1884=)

dbSNP: rs200662317
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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 RCV002160690 SCV002465941 likely benign Hypertrophic cardiomyopathy 14 2020-11-03 criteria provided, single submitter clinical testing

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