ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2149-8C>T

dbSNP: rs397515950
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000875086 SCV001017361 likely benign Hypertrophic cardiomyopathy 2023-04-17 criteria provided, single submitter clinical testing
GeneDx RCV002225758 SCV002504452 likely benign not provided 2020-01-16 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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