ClinVar Miner

Submissions for variant NM_006393.3(NEBL):c.259-8T>C

gnomAD frequency: 0.00005  dbSNP: rs753391210
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000864516 SCV001005326 likely benign Primary dilated cardiomyopathy 2022-12-26 criteria provided, single submitter clinical testing

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