ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.3300G>A (p.Gln1100=)

dbSNP: rs376802694
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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 RCV001480561 SCV001684881 likely benign Hypertrophic cardiomyopathy 14 2023-07-17 criteria provided, single submitter clinical testing

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