ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.1625-2A>G

dbSNP: rs112917345
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Total submissions: 1
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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 RCV000845293 SCV000987322 likely pathogenic not provided 2016-12-22 criteria provided, single submitter clinical testing

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