ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.3979-13C>G

dbSNP: rs563648655
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001722643 SCV000717672 likely benign not provided 2018-08-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003629120 SCV004403598 likely benign Hypertrophic cardiomyopathy 14 2024-07-08 criteria provided, single submitter clinical testing

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