ClinVar Miner

Submissions for variant NM_006393.3(NEBL):c.2868+19C>T

gnomAD frequency: 0.00001  dbSNP: rs41277364
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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 RCV002093248 SCV002375401 likely benign Primary dilated cardiomyopathy 2023-09-15 criteria provided, single submitter clinical testing

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