ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2869dup (p.Thr957fs)

dbSNP: rs876661365
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Stanford Center for Inherited Cardiovascular Disease, Stanford University RCV000223915 SCV000280246 likely pathogenic not provided 2012-06-20 no assertion criteria provided clinical testing Note this variant was found in clinical genetic testing performed by one or more labs who may also submit to ClinVar. Thus any internal case data may overlap with the internal case data of other labs. The interpretation reviewed below is that of the Stanford Center for Inherited Cardiovascular Disease

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