ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.1091-24C>T

gnomAD frequency: 0.22861  dbSNP: rs2856650
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000168765 SCV000303180 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001610477 SCV001840345 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001775657 SCV002014344 benign Left ventricular noncompaction 10 2021-09-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001775656 SCV002014345 benign Hypertrophic cardiomyopathy 4 2021-09-05 criteria provided, single submitter clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000168765 SCV001951880 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000168765 SCV001973887 benign not specified no assertion criteria provided clinical testing

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