ClinVar Miner

Submissions for variant NM_052867.4(NALCN):c.683_684dup (p.Cys229fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratoire de Génétique Moléculaire, CHU Bordeaux RCV001281633 SCV001468965 pathogenic not provided criteria provided, single submitter clinical testing

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