ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.3459A>G (p.Glu1153=)

dbSNP: rs2138593128
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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 RCV002076124 SCV002430295 likely benign Hypertrophic cardiomyopathy 14 2021-10-14 criteria provided, single submitter clinical testing

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