ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.1125G>A (p.Glu375=)

dbSNP: rs752309025
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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 RCV001424997 SCV001627607 likely benign Hypertrophic cardiomyopathy 14 2020-02-04 criteria provided, single submitter clinical testing

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