ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.855C>T (p.His285=)

gnomAD frequency: 0.00001  dbSNP: rs895857373
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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 RCV001410330 SCV001612376 likely benign Hypertrophic cardiomyopathy 14 2020-03-19 criteria provided, single submitter clinical testing

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