ClinVar Miner

Submissions for variant NM_001122630.2(CDKN1C):c.402G>A (p.Ala134=)

dbSNP: rs1848955478
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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 RCV001450105 SCV001653702 likely benign Beckwith-Wiedemann syndrome 2023-03-26 criteria provided, single submitter clinical testing

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