ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.579G>T (p.Pro193=)

dbSNP: rs794726872
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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 RCV002084030 SCV002430200 likely benign Beckwith-Wiedemann syndrome 2021-11-08 criteria provided, single submitter clinical testing

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