ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.66C>T (p.Leu22=)

dbSNP: rs960994716
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000873484 SCV001015479 likely benign Beckwith-Wiedemann syndrome 2023-07-16 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001817027 SCV002065765 likely benign not specified 2021-12-10 criteria provided, single submitter clinical testing

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