ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.765G>A (p.Lys255=)

dbSNP: rs1590148866
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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 RCV000928179 SCV001073786 likely benign Beckwith-Wiedemann syndrome 2023-06-28 criteria provided, single submitter clinical testing

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