ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.202-11G>A

dbSNP: rs374248120
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001697560 SCV000718591 likely benign not provided 2021-02-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002063171 SCV002442453 likely benign Hypertrophic cardiomyopathy 14 2024-11-16 criteria provided, single submitter clinical testing

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