ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2268T>C (p.Pro756=)

dbSNP: rs1595844260
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002149651 SCV002416497 likely benign Hypertrophic cardiomyopathy 2021-09-15 criteria provided, single submitter clinical testing

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