ClinVar Miner

Submissions for variant NM_002465.4(MYBPC1):c.1928-19T>G

gnomAD frequency: 0.00307  dbSNP: rs189706863
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251667 SCV000308890 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001558783 SCV001780800 likely benign not provided 2020-01-06 criteria provided, single submitter clinical testing

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