ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.666C>T (p.Arg222=)

dbSNP: rs779975908
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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 RCV001506828 SCV001711764 likely benign Beckwith-Wiedemann syndrome 2023-06-04 criteria provided, single submitter clinical testing

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