ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.546_587dup (p.Val184_Pro197dup)

dbSNP: rs2133783134
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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 RCV001417564 SCV001619768 likely benign Beckwith-Wiedemann syndrome 2023-09-21 criteria provided, single submitter clinical testing

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