ClinVar Miner

Submissions for variant NM_006393.3(NEBL):c.480+3069G>A

gnomAD frequency: 0.55177  dbSNP: rs3858198
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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 RCV002188579 SCV002485941 benign Primary dilated cardiomyopathy 2025-02-03 criteria provided, single submitter clinical testing

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