ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.5251A>C (p.Arg1751=)

dbSNP: rs1555333151
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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 RCV000647081 SCV000768868 likely benign Hypertrophic cardiomyopathy 14 2017-10-20 criteria provided, single submitter clinical testing

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