ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.2808G>C (p.Ala936=)

dbSNP: rs753515476
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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 RCV001452345 SCV001656003 likely benign Hypertrophic cardiomyopathy 14 2020-08-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704567 SCV005211376 likely benign not provided criteria provided, single submitter not provided

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