ClinVar Miner

Submissions for variant NM_144573.4(NEXN):c.865-17A>G

gnomAD frequency: 0.00016  dbSNP: rs201771600
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001529710 SCV001849644 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002070371 SCV002330680 likely benign Dilated cardiomyopathy 1CC; Hypertrophic cardiomyopathy 20 2024-10-23 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529710 SCV001743629 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001699811 SCV001918860 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001529710 SCV001927824 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001529710 SCV001956412 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001529710 SCV001969484 likely benign not provided no assertion criteria provided clinical testing

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