ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2535C>A (p.Arg845=)

dbSNP: rs1288578869
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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 RCV001181828 SCV001347067 likely benign Cardiomyopathy 2019-06-30 criteria provided, single submitter clinical testing
Invitae RCV001427987 SCV001630678 likely benign Hypertrophic cardiomyopathy 2019-07-01 criteria provided, single submitter clinical testing

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