ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.1530C>T (p.His510=)

dbSNP: rs2095889975
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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 RCV002169197 SCV002475401 likely benign Hypertrophic cardiomyopathy 2023-08-25 criteria provided, single submitter clinical testing

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