ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.1622dup (p.Glu542fs)

dbSNP: rs1555122143
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute RCV000627162 SCV000748016 likely pathogenic not provided 2017-02-23 criteria provided, single submitter clinical testing
Blueprint Genetics RCV000627162 SCV000927149 pathogenic not provided 2017-02-09 criteria provided, single submitter clinical testing

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