ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2013C>T (p.Val671=)

dbSNP: rs1168755518
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000774335 SCV000908037 likely benign Cardiomyopathy 2018-10-17 criteria provided, single submitter clinical testing
Invitae RCV002534134 SCV002941700 likely benign Hypertrophic cardiomyopathy 2022-03-02 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001701440 SCV001921726 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702716 SCV001931757 likely benign not provided no assertion criteria provided clinical testing

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