ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.432_503del (p.Val154_Pro177del)

dbSNP: rs2133784058
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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 RCV001436884 SCV001639729 likely benign Beckwith-Wiedemann syndrome 2020-09-01 criteria provided, single submitter clinical testing

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