ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.5566-7C>T

gnomAD frequency: 0.00029  dbSNP: rs200509899
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001707646 SCV000727114 likely benign not provided 2019-05-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000647090 SCV000768877 likely benign Hypertrophic cardiomyopathy 14 2024-08-31 criteria provided, single submitter clinical testing

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