ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2308+18C>G (rs3729948)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000168797 SCV000303187 benign not specified criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory,University Medical Center Utrecht RCV000616888 SCV000743555 benign Familial hypertrophic cardiomyopathy 4 2017-07-28 criteria provided, single submitter clinical testing
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000616888 SCV000744841 benign Familial hypertrophic cardiomyopathy 4 2015-09-21 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000616888 SCV000733042 benign Familial hypertrophic cardiomyopathy 4 no assertion criteria provided clinical testing

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