ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.516_545del (p.168AP[3])

dbSNP: rs1848940267
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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 RCV001499258 SCV001704019 likely benign Beckwith-Wiedemann syndrome 2022-03-05 criteria provided, single submitter clinical testing

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