ClinVar Miner

Submissions for variant NM_002472.3(MYH8):c.1663C>T (p.Leu555=)

gnomAD frequency: 0.00001  dbSNP: rs1481974689
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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 RCV000942925 SCV001088862 likely benign not provided 2018-08-15 criteria provided, single submitter clinical testing

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