ClinVar Miner

Submissions for variant NM_032578.4(MYPN):c.903-18A>T

gnomAD frequency: 0.00001  dbSNP: rs775857947
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002543880 SCV002981569 likely benign Dilated cardiomyopathy 1KK 2022-10-13 criteria provided, single submitter clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001723493 SCV001953733 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001723493 SCV001968881 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001729971 SCV001979141 benign not specified no assertion criteria provided clinical testing

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