ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.2175C>T (p.Arg725=)

gnomAD frequency: 0.00001  dbSNP: rs768890448
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001395689 SCV001597403 likely benign Hypertrophic cardiomyopathy 14 2023-06-01 criteria provided, single submitter clinical testing
GeneDx RCV001558888 SCV001780923 likely benign not provided 2021-05-27 criteria provided, single submitter clinical testing

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