ClinVar Miner

Submissions for variant NM_006393.3(NEBL):c.591C>T (p.Tyr197=)

gnomAD frequency: 0.00001  dbSNP: rs773877708
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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 RCV001478340 SCV001682610 likely benign Primary dilated cardiomyopathy 2019-08-06 criteria provided, single submitter clinical testing

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