ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.5589G>A (p.Leu1863=)

dbSNP: rs2138579438
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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 RCV001452178 SCV001655834 likely benign Hypertrophic cardiomyopathy 14 2019-05-03 criteria provided, single submitter clinical testing

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