ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.1352-10G>A

dbSNP: rs745645848
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001179906 SCV001344707 likely benign Cardiomyopathy 2019-01-31 criteria provided, single submitter clinical testing
Invitae RCV001425434 SCV001628062 likely benign Hypertrophic cardiomyopathy 2023-05-23 criteria provided, single submitter clinical testing

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