ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.906-13T>C

gnomAD frequency: 0.00001  dbSNP: rs730881219
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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 RCV001179821 SCV001344604 likely benign Cardiomyopathy 2023-11-27 criteria provided, single submitter clinical testing
Invitae RCV002068257 SCV002444678 likely benign Hypertrophic cardiomyopathy 2023-11-24 criteria provided, single submitter clinical testing

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