ClinVar Miner

Submissions for variant NM_006393.3(NEBL):c.1689A>G (p.Glu563=)

gnomAD frequency: 0.00003  dbSNP: rs1423516014
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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 RCV001498293 SCV001703039 likely benign Primary dilated cardiomyopathy 2022-02-10 criteria provided, single submitter clinical testing

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